Canonical Allele Identifier: PA2827312678
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2815206
ClinVar RCV Id: RCV003655713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Leu19Val
CA386776204
NM_001330437.2:c.55C>G