Canonical Allele Identifier: PA2829478339
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2963024
ClinVar RCV Id: RCV003828134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Leu53Pro
CA355516395
NM_004122.2:c.158T>C