Canonical Allele Identifier: PA2829385392
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440650
ClinVar RCV Id: RCV001950464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Ala461Val
CA386778105
NM_002834.5:c.1382C>T