Canonical Allele Identifier: PA2828894697
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369301
ClinVar RCV Id: RCV001874630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Gly597Val
CA346365375
NM_001382395.1:c.1790G>T