Canonical Allele Identifier: PA891861162
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 586562
ClinVar RCV Id: RCV000713245 RCV001515206
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092871.1:p.Asp433Asn
CA4348584
NM_001099401.2:c.1297G>A