Canonical Allele Identifier: PA2580238856
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_001369584.2:p.Ser412Leu
CA4304017
NM_001382655.3:c.1235C>T