Canonical Allele Identifier: PA2829478379
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2474012
ClinVar RCV Id: RCV003198155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Ser123Arg
CA355514864
NM_004122.2:c.369T>G
CA355514866
NM_004122.2:c.369T>A
CA355514875
NM_004122.2:c.367A>C