Canonical Allele Identifier: PA2825667027
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 464023
ClinVar RCV Id: RCV000524650 RCV001152446 RCV003139765
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Ala277Thr
CA3530706
NM_001128209.2:c.829G>A