Canonical Allele Identifier: PA2829478373
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2719344
ClinVar RCV Id: RCV003553606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Lys117Thr
CA355514942
NM_004122.2:c.350A>C