Canonical Allele Identifier: PA645439118
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 254721
ClinVar RCV Id: RCV000243208 RCV000665313 RCV001123794 RCV001508812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg221His
CA8643860
NM_000023.3:c.662G>A