Canonical Allele Identifier: PA915977655
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 286049
ClinVar RCV Id: RCV000341255 RCV000725776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Glu137Lys
CA501039
NM_001135697.3:c.409G>A