Canonical Allele Identifier: PA2827383351
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 2731847
ClinVar RCV Id: RCV003506461
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333648.1:p.Arg261Gly
CA4348701
NM_001346719.1:c.781C>G