Canonical Allele Identifier: PA2827312729
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40488
ClinVar Variation Id: 40489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asn58Lys
CA235313
NM_001330437.2:c.174C>A
CA261561
NM_001330437.2:c.174C>G