Canonical Allele Identifier: PA916056535
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40522
ClinVar RCV Id: RCV000037658 RCV000153788 RCV000234910 RCV000477501 RCV000723292 RCV000988915 RCV001253554 RCV001536068 RCV002415447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Arg265Gln
CA234739
NM_080601.3:c.794G>A