Canonical Allele Identifier: PA915977499
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 286025
ClinVar RCV Id: RCV000384383 RCV003137892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Leu66His
CA501057
NM_001135697.3:c.197T>A