Canonical Allele Identifier: PA2827185887
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1444977
ClinVar RCV Id: RCV001992488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310012.1:p.Ala156Gly
CA5412248
NM_001323083.2:c.467C>G