Canonical Allele Identifier: PA220235
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 92302
ClinVar RCV Id: RCV000077938 RCV001854369
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg81Cys
CA220233
NM_000023.3:c.241C>T