Canonical Allele Identifier: PA220238
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 92303
ClinVar RCV Id: RCV000077939 RCV000391706 RCV000852722 RCV001437168 RCV003915047 RCV004019523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg110Trp
CA220236
NM_000023.3:c.328C>T