Canonical Allele Identifier: PA2828066572
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1413798
ClinVar RCV Id: RCV001928316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349737.1:p.Ser234Leu
CA162922119
NM_001362808.2:c.701C>T