Canonical Allele Identifier: PA2827313069
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40518
ClinVar RCV Id: RCV000157681 RCV000033497 RCV000585640 RCV000506790 RCV000824743 RCV002399353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gln256Arg
CA235325
NM_001330437.2:c.767A>G