Canonical Allele Identifier: PA2573215944
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 1336032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369584.2:p.Thr387Met
CA4303992
NM_001382655.3:c.1160C>T