Canonical Allele Identifier: PA2828913770
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 2063877
ClinVar RCV Id: RCV002943033
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369591.2:p.Ser394Leu
CA4304017
NM_001382662.3:c.1181C>T