Canonical Allele Identifier: PA2825133412
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 959625
ClinVar RCV Id: RCV001233009 RCV003166428
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Val141Leu
CA362010420
NM_000337.6:c.421G>C
CA362010422
NM_000337.6:c.421G>T