Allele Registry

Canonical Allele Identifier: PA2827312756

Gene: PTPN11 HGNC NCBI

ClinVar RCV:

RCV000687319

ClinVar Variation:

40496

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317366.1:p.Asp61Val	CA282073 NM_001330437.2:c.182A>T