Allele Registry

Canonical Allele Identifier: PA2828530636

Gene: PTPN11 HGNC NCBI

ClinVar Variation Id: 620593

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361554.1:p.Phe313Leu	CA243712000 NM_001374625.1:c.937T>C CA386791017 NM_001374625.1:c.939T>A CA386791020 NM_001374625.1:c.939T>G