Canonical Allele Identifier: PA658800167
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 538663
ClinVar RCV Id: RCV000648062 RCV001288754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Gly17Arg
CA8643683
NM_000023.3:c.49G>A
CA400176330
NM_000023.3:c.49G>C