Canonical Allele Identifier: PA104919
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40670
ClinVar RCV Id: RCV001002596 RCV001217212 RCV002467510 RCV003460541 RCV001508984
ClinVar Variation Id: 40672
ClinVar RCV Id: RCV000038514 RCV000626886 RCV000781878 RCV000788323 RCV000856735 RCV001270835 RCV001526663 RCV001813286 RCV002054543 RCV002381284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Gly434Arg
CA261717
NM_005633.4:c.1300G>A
CA346366484
NM_005633.4:c.1300G>C