Canonical Allele Identifier: PA2580337568
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1729628
ClinVar RCV Id: RCV002325005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Thr1091Ala
CA389640469
NM_006939.4:c.3271A>G