Canonical Allele Identifier: PA645439221
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 373239
ClinVar RCV Id: RCV000413165 RCV003505108
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003910.1:p.Pro437Leu
CA4348533
NM_003919.3:c.1310C>T