Canonical Allele Identifier: PA645439049
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 286025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Leu66His
CA501057
NM_000023.3:c.197T>A