Canonical Allele Identifier: PA136096
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40697
ClinVar RCV Id: RCV000038529 RCV000206629 RCV000224003 RCV000272488 RCV000852769 RCV001094653 RCV001258236 RCV001813293 RCV002415454 RCV002496503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Ala708Thr
CA136094
NM_005633.4:c.2122G>A