Canonical Allele Identifier: PA2499303679
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1049115
ClinVar RCV Id: RCV001354790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940799.1:p.Asp32Glu
CA355516701
NM_198407.2:c.96C>G
CA355516702
NM_198407.2:c.96C>A