Canonical Allele Identifier: PA205478
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40722
ClinVar RCV Id: RCV000192568 RCV000997119 RCV000819933 RCV001143048 RCV001143049 RCV002444457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Pro1090Leu
CA205476
NM_005633.4:c.3269C>T