Canonical Allele Identifier: PA915977604
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 497191
ClinVar RCV Id: RCV000597853 RCV000872896 RCV001090957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Arg110Gln
CA8643771
NM_001135697.3:c.329G>A