Canonical Allele Identifier: PA916056622
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 520295
ClinVar RCV Id: RCV000619897 RCV003767818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Arg343Trp
CA386791486
NM_080601.3:c.1027C>T