Canonical Allele Identifier: PA2827312895
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 561745
ClinVar RCV Id: RCV000681127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Glu110Asp
CA386778519
NM_001330437.2:c.330A>C
CA386778523
NM_001330437.2:c.330A>T