Canonical Allele Identifier: PA2499303680
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1187869
ClinVar RCV Id: RCV001547453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940799.1:p.Arg141Leu
CA355514544
NM_198407.2:c.422G>T