Canonical Allele Identifier: PA2825667012
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 449229
ClinVar RCV Id: RCV000730461 RCV000695524 RCV001194184 RCV002527569
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Val264Ile
CA3530698
NM_001128209.2:c.790G>A