Canonical Allele Identifier: PA2573164695
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 1380499
ClinVar RCV Id: RCV001886380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Asn246Tyr
CA2918307
NM_000232.5:c.736A>T