Canonical Allele Identifier: PA2825536369
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 5773
ClinVar RCV Id: RCV000006129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092870.1:p.Leu196Arg
CA253601
NM_001099400.2:c.587T>G