Canonical Allele Identifier: PA105077
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40678
ClinVar RCV Id: RCV000038515 RCV000153986 RCV000623399 RCV000654915 RCV000763087 RCV001813287 RCV002054544 RCV003450659
ClinVar Variation Id: 40679
ClinVar RCV Id: RCV000159171 RCV001261087 RCV001381689 RCV002467514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Ser548Arg
CA234977
NM_005633.4:c.1642A>C
CA297272
NM_005633.4:c.1644T>A
CA346365700
NM_005633.4:c.1644T>G