Canonical Allele Identifier: PA282122
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40545
ClinVar RCV Id: RCV000033528 RCV001725940 RCV001852677 RCV001813255 RCV001818207 RCV004018713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Val428Met
CA282120
NM_002834.5:c.1282G>A