Canonical Allele Identifier: PA2827313098
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 44614
ClinVar RCV Id: RCV000037659 RCV000159050 RCV000587886 RCV001330780 RCV002504894 RCV003338391 RCV002415470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gly268Ser
CA261594
NM_001330437.2:c.802G>A