Canonical Allele Identifier: PA916056382
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13349
ClinVar RCV Id: RCV000014277 RCV000033445 RCV000211847 RCV000988912 RCV000694389 RCV002496356 RCV003156060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Thr2Ile
CA256764
NM_080601.3:c.5C>T