Canonical Allele Identifier: PA2827313217
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 181766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Arg343Gln
CA297648
NM_001330437.2:c.1028G>A