Canonical Allele Identifier: PA2826865228
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_001288068.1:p.Asn364Ser
CA368228891
NM_001301139.2:c.1091A>G