Canonical Allele Identifier: PA2829478385
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1209321
ClinVar RCV Id: RCV001577947 RCV003130539 RCV002568503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Arg141Pro
CA2706476
NM_004122.2:c.422G>C