Canonical Allele Identifier: PA220142
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40562
ClinVar RCV Id: RCV000033549 RCV000077853 RCV000156983 RCV000677652 RCV000762887 RCV001027841 RCV002390132 RCV003991572 RCV004532496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Met504Val
CA220140
NM_002834.5:c.1510A>G