Canonical Allele Identifier: PA913193909
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 633380
ClinVar RCV Id: RCV000781772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Ser499Thr
CA386779812
NM_002834.5:c.1495T>A