Canonical Allele Identifier: PA261716
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Thr378Ala
CA261714
NM_005633.4:c.1132A>G