Canonical Allele Identifier: PA645461692
Gene: CYP2U1 HGNC NCBI

Linked Data

ClinVar Variation Id: 409955
ClinVar RCV Id: RCV000466558 RCV001333700 RCV001848810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898898.1:p.Pro103Leu
CA3036967
NM_183075.3:c.308C>T