Canonical Allele Identifier: PA2827312730
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asn58His
CA235310
NM_001330437.2:c.172A>C