Canonical Allele Identifier: PA2827313136
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1327572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.His287Pro
CA386790444
NM_001330437.2:c.860A>C