Canonical Allele Identifier: PA275902
Gene: GRHPR HGNC NCBI

Linked Data

ClinVar Variation Id: 204240
ClinVar RCV Id: RCV000186447
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Amino-acid Alleles

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