Canonical Allele Identifier: PA2826667106
Gene: EXOSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 446202
ClinVar RCV Id: RCV000515461 RCV002527440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269638.1:p.Gly30Val
CA5284733
NM_001282709.1:c.89G>T