Canonical Allele Identifier: PA916029006
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 648594
ClinVar RCV Id: RCV000803351
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333642.1:p.Asn441Ser
CA368228891
NM_001346713.1:c.1322A>G