Canonical Allele Identifier: PA2828761541
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 1347977
ClinVar RCV Id: RCV002044098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365376.1:p.Asp443Val
CA350903329
NM_001378447.1:c.1328A>T