Canonical Allele Identifier: PA2828530600
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Phe284Ser
CA204408
NM_001374625.1:c.851T>C