Canonical Allele Identifier: PA2828894780
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40696
ClinVar RCV Id: RCV000156979 RCV000159124 RCV000817385 RCV002496502 RCV002467518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Tyr702His
CA273696
NM_001382395.1:c.2104T>C