Allele Registry

Canonical Allele Identifier: PA261589

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

48977

ClinVar RCV:

RCV000033484

RCV000037645

RCV000589214

RCV000815390

RCV001813248

ClinVar Variation:

40507

HGVS (amino-acid)	Matching Registered Transcripts
NP_002825.3:p.Glu110Lys	CA261587 NM_002834.5:c.328G>A