Canonical Allele Identifier: PA275892
Gene: GRHPR HGNC NCBI

Linked Data

ClinVar Variation Id: 204235
ClinVar RCV Id: RCV000186442 RCV000585941 RCV000802868 RCV003927729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036335.1:p.Gly165Asp
CA275891
NM_012203.2:c.494G>A