Canonical Allele Identifier: PA297300
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40647
ClinVar RCV Id: RCV000159187
ClinVar Variation Id: 40648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Trp85Arg
CA297298
NM_005633.4:c.253T>A
CA346373979
NM_005633.4:c.253T>C