Canonical Allele Identifier: PA261545
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Pro491Ser
CA261543
NM_002834.5:c.1471C>T