Allele Registry

Canonical Allele Identifier: PA282069

Gene: PTPN11 HGNC NCBI

ClinVar RCV:

RCV000033460

ClinVar Variation:

40492

HGVS (amino-acid)	Matching Registered Transcripts
NP_002825.3:p.Gly60_Asp61delinsVal	CA282067 NM_002834.5:c.179_182delinsT