Canonical Allele Identifier: PA2742032607
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 2858683
ClinVar RCV Id: RCV003699493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940799.1:p.Phe93Ser
CA355515754
NM_198407.2:c.278T>C