Canonical Allele Identifier: PA261596
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 44614
ClinVar RCV Id: RCV000037659 RCV000159050 RCV000587886 RCV001330780 RCV002504894 RCV003338391 RCV002415470
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Gly268Ser
CA261594
NM_002834.5:c.802G>A