Canonical Allele Identifier: PA2829641205
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1922339
ClinVar RCV Id: RCV002621584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006205.1:p.Arg245Trp
CA5412247
NM_006214.4:c.733C>T