Canonical Allele Identifier: PA2827312712
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1212983
ClinVar RCV Id: RCV001586630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gly49Arg
CA386777382
NM_001330437.2:c.145G>C
CA386777384
NM_001330437.2:c.145G>A