Canonical Allele Identifier: PA658665510
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 448352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg117Trp
CA8643775
NM_000023.3:c.349C>T