Canonical Allele Identifier: PA2827312754
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40495
ClinVar Variation Id: 372703
ClinVar RCV Id: RCV000412983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asp61Asn
CA235316
NM_001330437.2:c.181G>A
CA16042833
NM_001330437.2:c.180_181delinsAA