Canonical Allele Identifier: PA2825253114
Gene: EXOSC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001002269.1:p.Asp132Ala
CA204654
NM_001002269.2:c.395A>C