Allele Registry

Canonical Allele Identifier: PA2827185418

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008024

ClinVar Variation:

7586

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310009.1:p.Gln76Lys	CA118906 NM_001323080.2:c.226C>A