Canonical Allele Identifier: PA2573202528
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_001317366.1:p.Ala465Val
CA386778105
NM_001330437.2:c.1394C>T