Canonical Allele Identifier: PA658684539
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 496185
ClinVar RCV Id: RCV000590078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Val290Ile
CA386790490
NM_002834.5:c.868G>A