Canonical Allele Identifier: PA2828761122
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 2582384
ClinVar RCV Id: RCV003333365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365374.1:p.Lys513_Gly514del
CA2577269641
NM_001378445.1:c.1538_1543del