Canonical Allele Identifier: PA2829527639
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503128
ClinVar RCV Id: RCV002022668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004501.4:p.Ser171Arg
CA350916348
NM_004510.4:c.513T>G
CA350916350
NM_004510.4:c.513T>A
CA350916362
NM_004510.4:c.511A>C