Canonical Allele Identifier: PA134667
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 44607
ClinVar RCV Id: RCV000037646 RCV000680297 RCV000621552 RCV000654924 RCV000678902 RCV001813328 RCV002496598 RCV004534799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Lys131Arg
CA134665
NM_002834.5:c.392A>G