Allele Registry

Canonical Allele Identifier: PA916026806

Gene: PHYH HGNC NCBI

ClinVar Allele:

309753

ClinVar RCV:

RCV000319288

RCV000960582

RCV003930251

ClinVar Variation:

299255

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310013.1:p.Thr19Met	CA5412402 NM_001323084.2:c.56C>T