Canonical Allele Identifier: PA2826667128
Gene: EXOSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024889
ClinVar RCV Id: RCV001325128 RCV004035150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269638.1:p.Arg62Thr
CA5284767
NM_001282709.1:c.185G>C