Canonical Allele Identifier: PA2742032602
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2615765
ClinVar RCV Id: RCV003379191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940799.1:p.Glu73Gln
CA87786003
NM_198407.2:c.217G>C