Canonical Allele Identifier: PA2828893145
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1708841
ClinVar RCV Id: RCV002288125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Arg210Ser
CA346373052
NM_001382394.1:c.630G>T
CA346373053
NM_001382394.1:c.630G>C