Canonical Allele Identifier: PA2829384379
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1706401
ClinVar RCV Id: RCV002284931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Ala31Ser
CA386776280
NM_002834.5:c.91G>T