Canonical Allele Identifier: PA916028143
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Pro495Leu
CA273407
NM_001330437.2:c.1484C>T