Canonical Allele Identifier: PA2829527971
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 2582384
ClinVar RCV Id: RCV003333365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004501.4:p.Lys507_Gly508del
CA2577269641
NM_004510.4:c.1520_1525del