Canonical Allele Identifier: PA2828761115
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 1973708
ClinVar RCV Id: RCV002736205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365374.1:p.Arg496Trp
CA2154483
NM_001378445.1:c.1486C>T