Canonical Allele Identifier: PA916056441
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 164997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Glu69Val
CA177668
NM_080601.3:c.206A>T