Canonical Allele Identifier: PA2580558082
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2047338
ClinVar RCV Id: RCV002904232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940799.1:p.Asp113His
CA355514992
NM_198407.2:c.337G>C