Canonical Allele Identifier: PA2827312862
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1698190
ClinVar RCV Id: RCV002269613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asp94Val
CA386778196
NM_001330437.2:c.281A>T