Allele Registry

Canonical Allele Identifier: PA916026800

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008018

RCV000255609

RCV000505105

RCV000665657

RCV002426496

ClinVar Variation:

7580

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310011.1:p.Arg277Trp	CA118904 NM_001323082.2:c.829C>T