Canonical Allele Identifier: PA2580107396
Gene: GCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 2377818
ClinVar RCV Id: RCV004209202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000151.1:p.Thr54Met
CA8842004
NM_000160.5:c.161C>T