Canonical Allele Identifier: PA2828912899
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 16907
ClinVar RCV Id: RCV000018406 RCV000018407 RCV002490385 RCV003150931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369587.2:p.Arg454His
CA257662
NM_001382658.3:c.1361G>A