Canonical Allele Identifier: PA645412441
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 285260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Met116Val
CA2918434
NM_000232.5:c.346A>G