Canonical Allele Identifier: PA099743
Gene: EXOSC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31692
ClinVar RCV Id: RCV000024370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057126.2:p.Trp238Arg
CA260047
NM_016042.4:c.712T>C
CA373474717
NM_016042.4:c.712T>A