Canonical Allele Identifier: PA261723
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45346
ClinVar RCV Id: RCV000038517 RCV001813355 RCV002467541 RCV002467542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Cys471Ser
CA261721
NM_005633.4:c.1412G>C
CA346366229
NM_005633.4:c.1411T>A