Canonical Allele Identifier: PA2829527336
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_004500.4:p.Arg490Trp
CA2154483
NM_004509.5:c.1468C>T