Canonical Allele Identifier: PA261602
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40526
ClinVar RCV Id: RCV000033506 RCV000037661 RCV001027860 RCV001852676 RCV002444454
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Ile282Met
CA261600
NM_002834.5:c.846C>G