Canonical Allele Identifier: PA354984
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 224415
ClinVar RCV Id: RCV000210044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Lys91Arg
CA354982
NM_002834.5:c.272A>G