Canonical Allele Identifier: PA2827383695
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1413798
ClinVar RCV Id: RCV001928316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333649.1:p.Ser234Leu
CA162922119
NM_001346720.2:c.701C>T