Allele Registry

Canonical Allele Identifier: PA916028177

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

175398

ClinVar RCV:

RCV000154538

RCV000515184

RCV000680301

RCV000690056

RCV002399540

ClinVar Variation:

177887

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317366.1:p.Pro565Leu	CA180941 NM_001330437.2:c.1694C>T