Canonical Allele Identifier: PA2829182151
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2556267
ClinVar RCV Id: RCV004325059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376536.1:p.Gly1250Glu
CA352728636
NM_001389607.1:c.3749G>A