Canonical Allele Identifier: PA2828893478
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1499402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Glu555Asp
CA45674453
NM_001382394.1:c.1665G>C
CA346365618
NM_001382394.1:c.1665G>T