Canonical Allele Identifier: PA2829384695
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1305307
ClinVar RCV Id: RCV001768514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Thr168Ser
CA386781838
NM_002834.5:c.502A>T
CA386781842
NM_002834.5:c.503C>G