Canonical Allele Identifier: PA658654626
Gene: EXOSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 446202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055100.2:p.Gly30Val
CA5284733
NM_014285.7:c.89G>T