Canonical Allele Identifier: PA2827313240
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1009214
ClinVar RCV Id: RCV001306670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Lys364Arg
CA243712056
NM_001330437.2:c.1091A>G