Canonical Allele Identifier: PA356979
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 222972
ClinVar RCV Id: RCV000208567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Asp61del
CA356977
NM_002834.5:c.181_183del