Canonical Allele Identifier: PA2829245740
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 2071640
ClinVar RCV Id: RCV002975738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001382342.1:p.Val605Ile
CA4304308
NM_001395413.1:c.1813G>A