Canonical Allele Identifier: PA2828894338
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2752105
ClinVar RCV Id: RCV003540289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Arg227Ser
CA346372986
NM_001382395.1:c.681A>T
CA346372987
NM_001382395.1:c.681A>C