Canonical Allele Identifier: PA916063310
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 196256
ClinVar RCV Id: RCV000211553 RCV000666333 RCV000724012 RCV001043670 RCV003233485
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758447.1:p.Arg11Gln
CA302929
NM_172244.3:c.32G>A