Canonical Allele Identifier: PA916028177
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 177887
ClinVar RCV Id: RCV000154538 RCV000515184 RCV000680301 RCV000690056 RCV002399540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Pro565Leu
CA180941
NM_001330437.2:c.1694C>T