Canonical Allele Identifier: PA2828894526
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40670
ClinVar Variation Id: 40672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Gly434Arg
CA261717
NM_001382395.1:c.1300G>A
CA346366484
NM_001382395.1:c.1300G>C