Canonical Allele Identifier: PA2829478333
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2191613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Thr49Ile
CA2706523
NM_004122.2:c.146C>T