Canonical Allele Identifier: PA2827312791
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 44603
ClinVar RCV Id: RCV000037634 RCV000206837 RCV000405696 RCV002464090 RCV003313932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Lys70Arg
CA261568
NM_001330437.2:c.209A>G