Canonical Allele Identifier: PA211887
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 161391
ClinVar RCV Id: RCV000148887
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Gly76Cys
CA211885
NM_000337.6:c.226G>T