Canonical Allele Identifier: PA2828530466
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736690
ClinVar RCV Id: RCV002357735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Gly132Ser
CA386781003
NM_001374625.1:c.394G>A