Canonical Allele Identifier: PA2825133329
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2448149
ClinVar RCV Id: RCV003168198
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Lys92Glu
CA362008095
NM_000337.6:c.274A>G