Canonical Allele Identifier: PA915977536
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 9437
ClinVar RCV Id: RCV000010044 RCV000077937 RCV000779225 RCV001813971 RCV003987316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Arg77Cys
CA120427
NM_001135697.3:c.229C>T