Allele Registry

Canonical Allele Identifier: PA2827185698

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008024

ClinVar Variation:

7586

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310011.1:p.Gln178Lys	CA118906 NM_001323082.2:c.532C>A