Canonical Allele Identifier: PA916056580
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 496185
ClinVar RCV Id: RCV000590078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Val290Ile
CA386790490
NM_080601.3:c.868G>A