Canonical Allele Identifier: PA2829478369
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1915761
ClinVar RCV Id: RCV002594064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Trp109Arg
CA2706491
NM_004122.2:c.325T>C
CA355515039
NM_004122.2:c.325T>A