Allele Registry

Canonical Allele Identifier: PA2827312795

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

179444

ClinVar RCV:

RCV000159044

ClinVar Variation:

181495

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317366.1:p.Phe71Val	CA297073 NM_001330437.2:c.211T>G