Allele Registry

Canonical Allele Identifier: PA104827

Gene: SOS1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000013732

RCV000038525

RCV000149832

RCV000156992

RCV000159177

RCV000213008

RCV000515298

RCV000654947

RCV000763086

RCV000787997

RCV000787998

RCV000856746

RCV002250500

RCV002399362

RCV003128391

ClinVar Variation:

12872

40684

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005624.2:p.Arg552Ser	CA256580 NM_005633.4:c.1656G>C CA261730 NM_005633.4:c.1656G>T