Canonical Allele Identifier: PA2828912804
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 16902
ClinVar RCV Id: RCV000018401 RCV000170457 RCV000519572 RCV002243651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369587.2:p.Ala284Pro
CA257653
NM_001382658.3:c.850G>C