Canonical Allele Identifier: PA2828895055
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Pro1090Leu
CA205476
NM_001382395.1:c.3269C>T