Canonical Allele Identifier: PA2828530631
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Asn307Asp
CA220158
NM_001374625.1:c.919A>G