Canonical Allele Identifier: PA2499275397
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002804
ClinVar RCV Id: RCV001299278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Ile130Met
CA389649704
NM_006939.4:c.390T>G