Canonical Allele Identifier: PA2827313174
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asn308Asp
CA220158
NM_001330437.2:c.922A>G