Canonical Allele Identifier: PA2828895239
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 280339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Pro1259Arg
CA10602856
NM_001382395.1:c.3776C>G