Canonical Allele Identifier: PA2827313161
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Pro297Ala
CA386790612
NM_001330437.2:c.889C>G