Canonical Allele Identifier: PA2826666986
Gene: EXOSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1153205
ClinVar RCV Id: RCV001494802 RCV002284969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269637.1:p.Arg87Gln
CA5284789
NM_001282708.1:c.260G>A