Canonical Allele Identifier: PA2828530359
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40488
ClinVar Variation Id: 40489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Asn57Lys
CA235313
NM_001374625.1:c.171C>A
CA261561
NM_001374625.1:c.171C>G