Canonical Allele Identifier: PA2580362666
Gene: USP34 HGNC NCBI

Linked Data

ClinVar Variation Id: 2473611
ClinVar RCV Id: RCV004268640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055524.3:p.Ser355Leu
CA346974451
NM_014709.4:c.1064C>T