Canonical Allele Identifier: PA220157
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40528
ClinVar Variation Id: 44615
ClinVar Variation Id: 1201246
ClinVar RCV Id: RCV001566530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Phe285Leu
CA220155
NM_002834.5:c.853T>C
CA261606
NM_002834.5:c.855T>G
CA386790412
NM_002834.5:c.855T>A