Canonical Allele Identifier: PA256766
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13349
ClinVar RCV Id: RCV000014277 RCV000033445 RCV000211847 RCV000988912 RCV000694389 RCV002496356 RCV003156060
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Thr2Ile
CA256764
NM_002834.5:c.5C>T