Canonical Allele Identifier: PA915977683
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 498275
ClinVar RCV Id: RCV000592735 RCV001256191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Gly168Arg
CA8643815
NM_001135697.3:c.502G>A
CA400180003
NM_001135697.3:c.502G>C