Allele Registry

Canonical Allele Identifier: PA205478

Gene: SOS1 HGNC NCBI

ClinVar Allele:

49192

ClinVar RCV:

RCV000192568

RCV000819933

RCV000997119

RCV001143048

RCV001143049

RCV002444457

ClinVar Variation:

40722

HGVS (amino-acid)	Matching Registered Transcripts
NP_005624.2:p.Pro1090Leu	CA205476 NM_005633.4:c.3269C>T