Canonical Allele Identifier: PA2827312763
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 222972
ClinVar RCV Id: RCV000208567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asp61del
CA356977
NM_001330437.2:c.181_183del