Canonical Allele Identifier: PA261738
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45358
ClinVar RCV Id: RCV000038544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Tyr1008His
CA261736
NM_005633.4:c.3022T>C