Canonical Allele Identifier: PA2580502347
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1706401
ClinVar RCV Id: RCV002284931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Ala31Ser
CA386776280
NM_080601.3:c.91G>T