Allele Registry

Canonical Allele Identifier: PA916056453

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

48971

ClinVar RCV:

RCV000033474

RCV003152671

RCV003654180

ClinVar Variation:

40501

HGVS (amino-acid)	Matching Registered Transcripts
NP_542168.1:p.Thr73Pro	CA282079 NM_080601.3:c.217A>C