Canonical Allele Identifier: PA2827312719
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40485
ClinVar RCV Id: RCV000154561 RCV000557839 RCV000518841 RCV000788006 RCV000995619 RCV004528152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Ile56Val
CA180973
NM_001330437.2:c.166A>G