Canonical Allele Identifier: PA2828530369
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40492
ClinVar RCV Id: RCV000033460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Gly59_Asp60delinsVal
CA282067
NM_001374625.1:c.176_179delinsT