Canonical Allele Identifier: PA915977592
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 284685
ClinVar RCV Id: RCV000277867 RCV000725508 RCV001122686
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Ile103Val
CA8643746
NM_001135697.3:c.307A>G