Allele Registry

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Canonical Allele Identifier: PA2830155693

Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 1491431

ClinVar RCV Id: RCV001986519

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_536349.3:p.Gly494Arg	CA2154481 NM_080424.4:c.1480G>A CA350903323 NM_080424.4:c.1480G>C