Canonical Allele Identifier: PA2829384528
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516052
ClinVar RCV Id: RCV002048672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Asn92Lys
CA386778161
NM_002834.5:c.276T>A
CA386778163
NM_002834.5:c.276T>G