Canonical Allele Identifier: PA2828912659
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 469120
ClinVar RCV Id: RCV000549415 RCV002483455
ClinVar Variation Id: 2040336
ClinVar RCV Id: RCV002912476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369587.2:p.Phe69Leu
CA4303514
NM_001382658.3:c.205T>C
CA367747177
NM_001382658.3:c.207T>A
CA367747179
NM_001382658.3:c.207T>G