Canonical Allele Identifier: PA2829478353
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2615765
ClinVar RCV Id: RCV003379191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Glu73Gln
CA87786003
NM_004122.2:c.217G>C