Allele Registry

Canonical Allele Identifier: PA2827185782

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008020

RCV000117911

RCV000306854

ClinVar Variation:

7582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310012.1:p.Pro29Ser	CA154245 NM_001323083.2:c.85C>T