Canonical Allele Identifier: PA297075
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 181495
ClinVar RCV Id: RCV000159044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Phe71Val
CA297073
NM_002834.5:c.211T>G