Allele Registry

Canonical Allele Identifier: PA645433021

Gene: PHYH HGNC NCBI

ClinVar Allele:

309753

ClinVar RCV:

RCV000319288

RCV000960582

RCV003930251

ClinVar Variation:

299255

HGVS (amino-acid)	Matching Registered Transcripts
NP_006205.1:p.Thr119Met	CA5412402 NM_006214.4:c.356C>T