Canonical Allele Identifier: PA2827312741
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40492
ClinVar RCV Id: RCV000033460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gly60_Asp61delinsVal
CA282067
NM_001330437.2:c.179_182delinsT