Canonical Allele Identifier: PA645294406
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Ala72Pro
CA261571
NM_080601.3:c.214G>C