Canonical Allele Identifier: PA2829478308
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1049115
ClinVar RCV Id: RCV001354790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Asp32Glu
CA355516701
NM_004122.2:c.96C>G
CA355516702
NM_004122.2:c.96C>A