Canonical Allele Identifier: PA2825227109
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 2063877
ClinVar RCV Id: RCV002943033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000932.3:p.Ser397Leu
CA4304017
NM_000941.3:c.1190C>T