Canonical Allele Identifier: PA2827312844
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2735977
ClinVar RCV Id: RCV003540157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gln79Pro
CA386777926
NM_001330437.2:c.236A>C