Canonical Allele Identifier: PA2828894521
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12873
ClinVar RCV Id: RCV000013733 RCV000159161 RCV000211853 RCV000818949
ClinVar Variation Id: 667413
ClinVar RCV Id: RCV000826185
ClinVar Variation Id: 1712183
ClinVar RCV Id: RCV002293901 RCV003655354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Trp432Arg
CA256582
NM_001382395.1:c.1294T>C
CA346366503
NM_001382395.1:c.1294T>A
CA915943756
NM_001382395.1:c.1293_1294delinsGA