Canonical Allele Identifier: PA916056511
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 164998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asn200Tyr
CA273218
NM_080601.3:c.598A>T