Canonical Allele Identifier: PA2827312758
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 179221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asp61Ala
CA273600
NM_001330437.2:c.182A>C