Canonical Allele Identifier: PA2829454126
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1413798
ClinVar RCV Id: RCV001928316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003910.1:p.Ser325Leu
CA162922119
NM_003919.3:c.974C>T