Canonical Allele Identifier: PA2828912402
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 1336032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369586.2:p.Thr369Met
CA4303992
NM_001382657.2:c.1106C>T