Canonical Allele Identifier: PA2828894712
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1781362
ClinVar RCV Id: RCV002413049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Tyr618Cys
CA346365242
NM_001382395.1:c.1853A>G