Canonical Allele Identifier: PA267622
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 120249
ClinVar RCV Id: RCV000106329 RCV000414070 RCV001344369 RCV002467565 RCV004019595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Arg713Gln
CA267620
NM_005633.4:c.2138G>A