Canonical Allele Identifier: PA2827312876
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2501368
ClinVar RCV Id: RCV003227163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Pro101Ser
CA386778322
NM_001330437.2:c.301C>T