Canonical Allele Identifier: PA916056453
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Thr73Pro
CA282079
NM_080601.3:c.217A>C