Canonical Allele Identifier: PA2827313173
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40535
ClinVar RCV Id: RCV000033517 RCV000037668 RCV001193110 RCV002287350 RCV002371807 RCV001813251 RCV002482942 RCV004532491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asn308Thr
CA261607
NM_001330437.2:c.923A>C