Canonical Allele Identifier: PA2573215957
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 16907
ClinVar RCV Id: RCV000018406 RCV000018407 RCV002490385 RCV003150931
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369584.2:p.Arg472His
CA257662
NM_001382655.3:c.1415G>A