Canonical Allele Identifier: PA2828530393
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 181495
ClinVar RCV Id: RCV000159044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Phe70Val
CA297073
NM_001374625.1:c.208T>G