Canonical Allele Identifier: PA2825005311
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2430699
ClinVar RCV Id: RCV003129232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Ala23Asp
CA400176450
NM_000023.3:c.68C>A