Canonical Allele Identifier: PA2828760164
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 2328387
ClinVar RCV Id: RCV002934904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365371.1:p.Thr501Pro
CA2154480
NM_001378442.1:c.1501A>C