Canonical Allele Identifier: PA2828530395
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Ala71Pro
CA261571
NM_001374625.1:c.211G>C