Allele Registry

Canonical Allele Identifier: PA2830155657

Gene: SP110 HGNC NCBI

ClinVar Allele:

20578

ClinVar RCV:

RCV000005877

RCV000455916

RCV001517855

ClinVar Variation:

5539

HGVS (amino-acid)	Matching Registered Transcripts
NP_536349.3:p.Leu425Ser	CA117579 NM_080424.4:c.1274T>C