Canonical Allele Identifier: PA099721
Gene: EXOSC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 31688
ClinVar RCV Id: RCV000024366 RCV000190687 RCV000224817 RCV000761614 RCV001836713 RCV003156064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057126.2:p.Asp132Ala
CA204654
NM_016042.4:c.395A>C