Canonical Allele Identifier: PA346679
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180531
ClinVar RCV Id: RCV000157508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Thr451Lys
CA346677
NM_005633.4:c.1352C>A