Canonical Allele Identifier: PA282069
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40492
ClinVar RCV Id: RCV000033460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Gly60_Asp61delinsVal
CA282067
NM_002834.5:c.179_182delinsT