Canonical Allele Identifier: PA261557
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40484
ClinVar RCV Id: RCV000033452 RCV000037621 RCV000809051 RCV002287349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Thr52Ile
CA261555
NM_002834.5:c.155C>T