Canonical Allele Identifier: PA2828912432
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 1204490
ClinVar RCV Id: RCV001570851 RCV002072208 RCV002246433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369586.2:p.Gly410Ser
CA4304036
NM_001382657.2:c.1228G>A