Canonical Allele Identifier: PA2742003785
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2501368
ClinVar RCV Id: RCV003227163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Pro101Ser
CA386778322
NM_080601.3:c.301C>T