Allele Registry

Canonical Allele Identifier: PA916056596

Gene: PTPN11 HGNC NCBI

ClinVar Variation Id: 620593

HGVS (amino-acid)	Matching Registered Transcripts
NP_542168.1:p.Phe314Leu	CA243712000 NM_080601.3:c.940T>C CA386791017 NM_080601.3:c.942T>A CA386791020 NM_080601.3:c.942T>G