Canonical Allele Identifier: PA2828530372
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40496
ClinVar RCV Id: RCV000687319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Asp60Val
CA282073
NM_001374625.1:c.179A>T