Allele Registry

Canonical Allele Identifier: PA645387018

Gene: SOS2 HGNC NCBI

ClinVar Variation Id: 280923

HGVS (amino-acid)	Matching Registered Transcripts
NP_008870.2:p.Asn993Ile	CA7176895 NM_006939.4:c.2978A>T