Canonical Allele Identifier: PA2827312775
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13329
ClinVar RCV Id: RCV000014257 RCV000033466 RCV000153794 RCV000156993 RCV000590972 RCV000762882 RCV000824739 RCV001813195 RCV002408460 RCV004532340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Tyr62Asp
CA234749
NM_001330437.2:c.184T>G