Canonical Allele Identifier: PA645294417
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_542168.1:p.Phe285Leu
CA220155
NM_080601.3:c.853T>C
CA261606
NM_080601.3:c.855T>G
CA386790412
NM_080601.3:c.855T>A