Canonical Allele Identifier: PA2827312885
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asp106Ala
CA261584
NM_001330437.2:c.317A>C