Canonical Allele Identifier: PA104827
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12872
ClinVar RCV Id: RCV000159177 RCV000156992 RCV000654947 RCV000763086 RCV000787998 RCV000856746 RCV000013732
ClinVar Variation Id: 40684
ClinVar RCV Id: RCV000038525 RCV000149832 RCV000515298 RCV000213008 RCV002250500 RCV002399362 RCV000787997 RCV003128391
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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