Canonical Allele Identifier: PA2827588000
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004334952
ClinVar Variation:
2591163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338036.1:p.Arg222Gln
CA2393313
NM_001351107.2:c.665G>A