Canonical Allele Identifier: PA2829478392
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1464940
ClinVar RCV Id: RCV001979247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Leu149Ile
CA355514464
NM_004122.2:c.445C>A