Canonical Allele Identifier: PA2742032617
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2802359
ClinVar RCV Id: RCV003668787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940799.1:p.Val170Met
CA355514298
NM_198407.2:c.508G>A