Canonical Allele Identifier: PA2828760789
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 957020
ClinVar RCV Id: RCV001229929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365373.1:p.Glu507Gly
CA350903269
NM_001378444.1:c.1520A>G