Canonical Allele Identifier: PA2828530427
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1698190
ClinVar RCV Id: RCV002269613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Asp93Val
CA386778196
NM_001374625.1:c.278A>T