Canonical Allele Identifier: PA2827312817
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Thr73Ile
CA256752
NM_001330437.2:c.218C>T