Canonical Allele Identifier: PA2827312889
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1803533
ClinVar RCV Id: RCV002467203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Thr108Ile
CA386778469
NM_001330437.2:c.323C>T