Canonical Allele Identifier: PA2827312645
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Thr2Ile
CA256764
NM_001330437.2:c.5C>T