Allele Registry

Canonical Allele Identifier: PA108249

Gene: PHYH HGNC NCBI

ClinVar Allele:

22619

ClinVar RCV:

RCV000008018

RCV000255609

RCV000505105

RCV000665657

RCV002426496

ClinVar Variation:

7580

HGVS (amino-acid)	Matching Registered Transcripts
NP_006205.1:p.Arg275Trp	CA118904 NM_006214.4:c.823C>T