Canonical Allele Identifier: PA099718
Gene: EXOSC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057126.2:p.Ala139Pro
CA260045
NM_016042.4:c.415G>C