Canonical Allele Identifier: PA2825133299
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1789219
ClinVar RCV Id: RCV002457534
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Leu77Ile
CA362007993
NM_000337.6:c.229C>A