Canonical Allele Identifier: PA2827312706
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40482
ClinVar RCV Id: RCV000157002 RCV000157675 RCV000227194 RCV001330777 RCV001813241 RCV002399352 RCV002482941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Thr42Ala
CA235307
NM_001330437.2:c.124A>G