Canonical Allele Identifier: PA104939
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2672811
ClinVar RCV Id: RCV003457065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Gly482Arg
CA346366159
NM_005633.4:c.1444G>C