Canonical Allele Identifier: PA2829385089
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1505187
ClinVar RCV Id: RCV002020412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Glu348Val
CA386791556
NM_002834.5:c.1043A>T