Canonical Allele Identifier: PA2580158516
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2430699
ClinVar RCV Id: RCV003129232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Ala23Asp
CA400176450
NM_001135697.3:c.68C>A