Allele Registry

Canonical Allele Identifier: PA108276

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008024

ClinVar Variation:

7586

HGVS (amino-acid)	Matching Registered Transcripts
NP_006205.1:p.Gln176Lys	CA118906 NM_006214.4:c.526C>A