Canonical Allele Identifier: PA916056480
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asp106Ala
CA261584
NM_080601.3:c.317A>C