Canonical Allele Identifier: PA2825666806
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 202086
ClinVar RCV Id: RCV000183900 RCV001852377 RCV003233488
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Val38Ala
CA308782
NM_001128209.2:c.113T>C