Canonical Allele Identifier: PA2827312725
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asn58Asp
CA261558
NM_001330437.2:c.172A>G