Canonical Allele Identifier: PA2580337381
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714619
ClinVar RCV Id: RCV002295710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Ile750Ser
CA389643871
NM_006939.4:c.2249T>G