Allele Registry

Canonical Allele Identifier: PA297072

Gene: PTPN11 HGNC NCBI

ClinVar RCV:

RCV000159042

RCV001174933

ClinVar Variation:

181494

HGVS (amino-acid)	Matching Registered Transcripts
NP_002825.3:p.Asn58Tyr	CA297070 NM_002834.5:c.172A>T