Canonical Allele Identifier: PA658665482
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 471336

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Asp20Asn
CA8643685
NM_000023.3:c.58G>A