Canonical Allele Identifier: PA2827313123
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Phe285Ser
CA204408
NM_001330437.2:c.854T>C