Canonical Allele Identifier: PA915996631
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 334902
ClinVar RCV Id: RCV000362881 RCV000455391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171944.1:p.Met529Thr
CA2154463
NM_001185015.2:c.1586T>C