Canonical Allele Identifier: PA658829360
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 561713
ClinVar RCV Id: RCV000681078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Glu523Asp
CA386780067
NM_002834.5:c.1569A>C
CA386780069
NM_002834.5:c.1569A>T