Canonical Allele Identifier: PA2827383456
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1059320
ClinVar RCV Id: RCV001368574
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333648.1:p.Pro371Ser
CA368228928
NM_001346719.1:c.1111C>T