Allele Registry

Canonical Allele Identifier: PA275902

Gene: GRHPR HGNC NCBI

ClinVar Allele:

200648

ClinVar RCV:

RCV000186447

ClinVar Variation:

204240

HGVS (amino-acid)	Matching Registered Transcripts
NP_036335.1:p.Met322Thr	CA275901 NM_012203.2:c.965T>C