Canonical Allele Identifier: PA2499249955
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1063416
ClinVar RCV Id: RCV001373249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333642.1:p.Pro435Ala
CA162920306
NM_001346713.1:c.1303C>G