Canonical Allele Identifier: PA916056472
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 224415
ClinVar RCV Id: RCV000210044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Lys91Arg
CA354982
NM_080601.3:c.272A>G