Canonical Allele Identifier: PA2828761132
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 334902
ClinVar RCV Id: RCV000362881 RCV000455391
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365374.1:p.Met529Thr
CA2154463
NM_001378445.1:c.1586T>C