Canonical Allele Identifier: PA2827312857
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1425818
ClinVar RCV Id: RCV001926935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gly86Arg
CA243707921
NM_001330437.2:c.256G>A
CA386778026
NM_001330437.2:c.256G>C