Canonical Allele Identifier: PA916056484
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 561745
ClinVar RCV Id: RCV000681127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Glu110Asp
CA386778519
NM_080601.3:c.330A>C
CA386778523
NM_080601.3:c.330A>T