Canonical Allele Identifier: PA261733
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40699
ClinVar RCV Id: RCV000038531 RCV000495874 RCV000159126 RCV001045366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Lys728Ile
CA261731
NM_005633.4:c.2183A>T