Canonical Allele Identifier: PA916063365
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 202090
ClinVar RCV Id: RCV000183904
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758447.1:p.Gly81del
CA308794
NM_172244.3:c.242_244del