Canonical Allele Identifier: PA645294548
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 228392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Asp61Tyr
CA10576907
NM_002834.5:c.181G>T
CA243707918
NM_002834.5:c.180_181delinsGT