Canonical Allele Identifier: PA2827312859
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516052
ClinVar RCV Id: RCV002048672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asn92Lys
CA386778161
NM_001330437.2:c.276T>A
CA386778163
NM_001330437.2:c.276T>G