Canonical Allele Identifier: PA2827313145
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 496185
ClinVar RCV Id: RCV000590078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Val290Ile
CA386790490
NM_001330437.2:c.868G>A