Canonical Allele Identifier: PA2828893460
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12872
ClinVar Variation Id: 40684

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Arg545Ser
CA256580
NM_001382394.1:c.1635G>C
CA261730
NM_001382394.1:c.1635G>T