Canonical Allele Identifier: PA2829447978
Gene: USP4 HGNC NCBI
ClinVar RCV:
RCV004315093
ClinVar Variation:
2546331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003354.2:p.Ser157Cys
CA352774134
NM_003363.4:c.469A>T