Canonical Allele Identifier: PA645439054
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 432007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Leu76Phe
CA400177503
NM_000023.3:c.226C>T