Allele Registry

Canonical Allele Identifier: PA2827186006

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008025

RCV003473055

ClinVar Variation:

7587

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310013.1:p.Gly106Ser	CA118907 NM_001323084.2:c.316G>A