Canonical Allele Identifier: PA658820380
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40488
ClinVar RCV Id: RCV000037629 RCV000157677 RCV000587067 RCV000556984 RCV001358687 RCV001813243
ClinVar Variation Id: 40489
ClinVar RCV Id: RCV000033457 RCV000037630 RCV000211846 RCV000515267 RCV000588173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asn58Lys
CA235313
NM_080601.3:c.174C>A
CA261561
NM_080601.3:c.174C>G