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Canonical Allele Identifier: Get Identifier
Gene: PHYH HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
ENSP00000420117.1:p.Gly206Ser
ENST00000479604.1:c.[616G>A;620G=]

ENST00000479604.1:c.[616G>A;621T>C]

ENST00000479604.1:c.[616G>A;621T=]

ENST00000479604.1:c.[616G>A;622C>T]

ENST00000479604.1:c.[616G>A;624G>A]

ENST00000479604.1:c.[616G>A;624G>C]

ENST00000479604.1:c.[616G>A;624G=]

ENST00000479604.1:c.[616G>A;624G>T]

ENST00000479604.1:c.[616G>A;625G=]

ENST00000479604.1:c.[616G>A;626T=]

ENST00000479604.1:c.[616G>A;627T>A]

ENST00000479604.1:c.[616G>A;627T>C]

ENST00000479604.1:c.[616G>A;627T>G]