Canonical Allele Identifier: PA2580337024
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1947234
ClinVar RCV Id: RCV002685447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Lys311Thr
CA389646978
NM_006939.4:c.932A>C