Canonical Allele Identifier: PA2829478389
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1962623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Phe147Tyr
CA2706471
NM_004122.2:c.440T>A