Canonical Allele Identifier: PA2828893030
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40647
ClinVar RCV Id: RCV000159187
ClinVar Variation Id: 40648
ClinVar RCV Id: RCV000545153 RCV001261068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Trp78Arg
CA297298
NM_001382394.1:c.232T>A
CA346373979
NM_001382394.1:c.232T>C