Canonical Allele Identifier: PA645294412
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40512
ClinVar Variation Id: 40513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Glu139Asp
CA177671
NM_080601.3:c.417G>C
CA261590
NM_080601.3:c.417G>T