Canonical Allele Identifier: PA2829478398
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1397925
ClinVar RCV Id: RCV001912672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Ile167Phe
CA2706457
NM_004122.2:c.499A>T