Canonical Allele Identifier: PA282081
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Thr73Pro
CA282079
NM_002834.5:c.217A>C