Canonical Allele Identifier: PA891866186
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13331
ClinVar RCV Id: RCV000033533 RCV000055884 RCV000077851 RCV000106323 RCV000157014 RCV000208002 RCV000515406 RCV000723326 RCV000853462 RCV001813197 RCV002390104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Thr472Met
CA220134
NM_001330437.2:c.1415C>T