Canonical Allele Identifier: PA2827312747
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gly60Ser
CA235370
NM_001330437.2:c.178G>A