Canonical Allele Identifier: PA2827312819
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40501
ClinVar RCV Id: RCV000033474 RCV003152671 RCV003654180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Thr73Pro
CA282079
NM_001330437.2:c.217A>C