Allele Registry

Canonical Allele Identifier: PA105097

Gene: SOS1 HGNC NCBI

ClinVar RCV:

RCV000159173

RCV000696409

RCV000780747

ClinVar Variation:

181553

HGVS (amino-acid)	Matching Registered Transcripts
NP_005624.2:p.Thr549Lys	CA297273 NM_005633.4:c.1646C>A