Canonical Allele Identifier: PA261605
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40533
ClinVar RCV Id: RCV000033513 RCV000037664 RCV000212895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Phe285Cys
CA261603
NM_002834.5:c.854T>G