Canonical Allele Identifier: PA091236
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 9437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg77Cys
CA120427
NM_000023.3:c.229C>T