Canonical Allele Identifier: PA104837
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40682
ClinVar RCV Id: RCV000159176 RCV000208093 RCV000528274 RCV000626887 RCV001507015 RCV001813288 RCV002399361 RCV003390718 RCV003450660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Arg552Thr
CA261728
NM_005633.4:c.1655G>C