Canonical Allele Identifier: PA658800179
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 538661
ClinVar RCV Id: RCV000648059
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Gly91Cys
CA291536150
NM_000023.3:c.271G>T