Canonical Allele Identifier: PA261573
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40500
ClinVar RCV Id: RCV000033472 RCV000037635 RCV001852674 RCV003103718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Ala72Pro
CA261571
NM_002834.5:c.214G>C