Allele Registry

Canonical Allele Identifier: PA2828530393

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

179444

ClinVar RCV:

RCV000159044

ClinVar Variation:

181495

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361554.1:p.Phe70Val	CA297073 NM_001374625.1:c.208T>G