Canonical Allele Identifier: PA2827312808
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Ala72Pro
CA261571
NM_001330437.2:c.214G>C