Canonical Allele Identifier: PA2827517951
Gene: SDCCAG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 296908
ClinVar RCV Id: RCV000342454 RCV000399034 RCV000522463 RCV000763845 RCV004537663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337177.1:p.Thr191Ile
CA1483350
NM_001350248.2:c.572C>T