Canonical Allele Identifier: PA2827312917
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736690
ClinVar RCV Id: RCV002357735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gly133Ser
CA386781003
NM_001330437.2:c.397G>A