Canonical Allele Identifier: PA2829478318
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 3009619
ClinVar RCV Id: RCV003864730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Gln36His
CA87786296
NM_004122.2:c.108G>C
CA355516653
NM_004122.2:c.108G>T