Allele Registry

Canonical Allele Identifier: PA2827186067

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008026

RCV001851728

RCV003473056

ClinVar Variation:

7588

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310013.1:p.Arg177Gln	CA118908 NM_001323084.2:c.530G>A