Allele Registry

Canonical Allele Identifier: PA220157

Gene: PTPN11 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

48998

53782

1191330

ClinVar RCV:

RCV000037662

RCV000037665

RCV000077861

RCV000159052

RCV000231840

RCV000586058

RCV000587757

RCV000687570

RCV000762885

RCV000856809

RCV001566530

RCV002288529

RCV002288537

RCV004018710

RCV004532490

ClinVar Variation:

40528

44615

1201246

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002825.3:p.Phe285Leu	CA220155 NM_002834.5:c.853T>C CA261606 NM_002834.5:c.855T>G CA386790412 NM_002834.5:c.855T>A