Canonical Allele Identifier: PA106805
Gene: CYP2U1 HGNC NCBI
ClinVar RCV:
RCV000032699
ClinVar Variation:
39503
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898898.1:p.Cys262Arg
CA130343
NM_183075.3:c.784T>C