Canonical Allele Identifier: PA2826666937
Gene: EXOSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 778382
ClinVar RCV Id: RCV000959014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269637.1:p.Pro8Ala
CA5284710
NM_001282708.1:c.22C>G