Canonical Allele Identifier: PA2828066653
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 373239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349737.1:p.Pro337Leu
CA4348533
NM_001362808.2:c.1010C>T