Allele Registry

Canonical Allele Identifier: PA916056400

Gene: PTPN11 HGNC NCBI

ClinVar RCV:

RCV000159042

RCV001174933

ClinVar Variation:

181494

HGVS (amino-acid)	Matching Registered Transcripts
NP_542168.1:p.Asn58Tyr	CA297070 NM_080601.3:c.172A>T