Canonical Allele Identifier: PA2827383453
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1063416
ClinVar RCV Id: RCV001373249
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333648.1:p.Pro370Ala
CA162920306
NM_001346719.1:c.1108C>G