Canonical Allele Identifier: PA2827383109
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_001333646.1:p.Asn396Ser
CA368228891
NM_001346717.1:c.1187A>G