Canonical Allele Identifier: PA2827312782
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 164997
ClinVar RCV Id: RCV000151687 RCV000589756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Glu69Val
CA177668
NM_001330437.2:c.206A>T