Canonical Allele Identifier: PA2827312787
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1997356
ClinVar RCV Id: RCV002823966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Glu69Ala
CA386777758
NM_001330437.2:c.206A>C