Allele Registry

Canonical Allele Identifier: PA916026798

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008022

ClinVar Variation:

7584

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310011.1:p.Asn271His	CA118905 NM_001323082.2:c.811A>C