Canonical Allele Identifier: PA2828530468
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40512
ClinVar Variation Id: 40513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Glu138Asp
CA177671
NM_001374625.1:c.414G>C
CA261590
NM_001374625.1:c.414G>T