Canonical Allele Identifier: PA2826865181
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 938661
ClinVar RCV Id: RCV001207926
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288068.1:p.Asn336His
CA4348623
NM_001301139.2:c.1006A>C