Canonical Allele Identifier: PA916028162
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gln514Pro
CA256758
NM_001330437.2:c.1541A>C