Canonical Allele Identifier: PA2828894670
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1328600
ClinVar RCV Id: RCV001797232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Leu569Pro
CA346365569
NM_001382395.1:c.1706T>C