Canonical Allele Identifier: PA916056447
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40499
ClinVar Variation Id: 477670
ClinVar Variation Id: 2582571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Phe71Leu
CA273215
NM_080601.3:c.211T>C
CA386777846
NM_080601.3:c.213T>A
CA386777847
NM_080601.3:c.213T>G