Canonical Allele Identifier: PA261542
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40549
ClinVar RCV Id: RCV000033535 RCV000694590 RCV000208219 RCV000660240 RCV002490445 RCV004018714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Pro491Thr
CA261540
NM_002834.5:c.1471C>A