Canonical Allele Identifier: PA2828894379
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Thr266Lys
CA256578
NM_001382395.1:c.797C>A