Canonical Allele Identifier: PA2828913318
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 911635
ClinVar RCV Id: RCV001164198 RCV001546288 RCV002483918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369588.2:p.Arg403His
CA4304027
NM_001382659.3:c.1208G>A