Allele Registry

Canonical Allele Identifier: PA282134

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

49031

ClinVar RCV:

RCV000033548

RCV000532971

RCV000677651

RCV001330778

RCV002490448

RCV003450655

ClinVar Variation:

40561

HGVS (amino-acid)	Matching Registered Transcripts
NP_002825.3:p.Gly503Glu	CA282132 NM_002834.5:c.1508G>A