Allele Registry

Canonical Allele Identifier: PA1139704377

Gene: SOS1 HGNC NCBI

ClinVar Allele:

969636

ClinVar RCV:

RCV001261085

ClinVar Variation:

981569

HGVS (amino-acid)	Matching Registered Transcripts
NP_005624.2:p.Asn508Asp	CA346365978 NM_005633.4:c.1522A>G