Canonical Allele Identifier: PA2828913013
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 2071640
ClinVar RCV Id: RCV002975738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369587.2:p.Val605Ile
CA4304308
NM_001382658.3:c.1813G>A