Canonical Allele Identifier: PA2826864800
Gene: SGCE HGNC NCBI

Linked Data

ClinVar Variation Id: 5773
ClinVar RCV Id: RCV000006129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288068.1:p.Leu155Arg
CA253601
NM_001301139.2:c.464T>G