Allele Registry

Canonical Allele Identifier: PA2825380833

Gene: PHYH HGNC NCBI

ClinVar Allele:

195700

ClinVar RCV:

RCV000179914

RCV000665931

RCV000755125

RCV000950185

RCV001258288

ClinVar Variation:

198539

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032626.1:p.Arg145Gln	CA203488 NM_001037537.2:c.434G>A