Canonical Allele Identifier: PA2826667087
Gene: EXOSC2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269638.1:p.Pro8Ala
CA5284710
NM_001282709.1:c.22C>G