Canonical Allele Identifier: PA2828751134
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 2065576
ClinVar RCV Id: RCV002958577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365174.1:p.Lys127Gln
CA6909658
NM_001378245.1:c.379A>C