Canonical Allele Identifier: PA2828530362
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Asn57His
CA235310
NM_001374625.1:c.169A>C