Canonical Allele Identifier: PA2826667173
Gene: EXOSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 446203
ClinVar RCV Id: RCV000515462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269638.1:p.Gly168Asp
CA375247996
NM_001282709.1:c.503G>A