Canonical Allele Identifier: PA2580291054
Gene: USP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2216001
ClinVar RCV Id: RCV004082765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003354.2:p.Glu691Asp
CA2396740
NM_003363.4:c.2073G>T
CA352781428
NM_003363.4:c.2073G>C