Canonical Allele Identifier: PA2825095747
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 289650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000222.2:p.Leu53Pro
CA10606508
NM_000231.3:c.158T>C