Allele Registry

Canonical Allele Identifier: PA916026791

Gene: PHYH HGNC NCBI

ClinVar Allele:

314641

ClinVar RCV:

RCV000267540

RCV000487565

ClinVar Variation:

299251

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310011.1:p.Arg203Gly	CA5412303 NM_001323082.2:c.607C>G