Canonical Allele Identifier: PA261567
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40498
ClinVar RCV Id: RCV000033469 RCV000037633 RCV000212889 RCV002415446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Glu69Gln
CA261565
NM_002834.5:c.205G>C