Canonical Allele Identifier: PA916013055
Gene: EXOSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 778382
ClinVar RCV Id: RCV000959014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055100.2:p.Pro8Ala
CA5284710
NM_014285.7:c.22C>G