Canonical Allele Identifier: PA2828066454
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 5773
ClinVar RCV Id: RCV000006129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349737.1:p.Leu105Arg
CA253601
NM_001362808.2:c.314T>G