Canonical Allele Identifier: PA2828530373
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 228392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Asp60Tyr
CA10576907
NM_001374625.1:c.178G>T
CA243707918
NM_001374625.1:c.177_178delinsGT