Allele Registry

Canonical Allele Identifier: PA916026808

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008024

ClinVar Variation:

7586

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310013.1:p.Gln78Lys	CA118906 NM_001323084.2:c.232C>A