Canonical Allele Identifier: PA915977695
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 288595
ClinVar RCV Id: RCV000486077 RCV000675090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Arg181Ser
CA8643819
NM_001135697.3:c.541C>A