Canonical Allele Identifier: PA177670
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 164997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Glu69Val
CA177668
NM_002834.5:c.206A>T