Canonical Allele Identifier: PA645294562
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 280278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Glu123Asp
CA6798547
NM_002834.5:c.369G>T
CA386780704
NM_002834.5:c.369G>C