Canonical Allele Identifier: PA2829527342
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 2328387
ClinVar RCV Id: RCV002934904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004500.4:p.Thr495Pro
CA2154480
NM_004509.5:c.1483A>C