Canonical Allele Identifier: PA2828912848
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 1336032
ClinVar RCV Id: RCV001822214 RCV001869654 RCV003238872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369587.2:p.Thr369Met
CA4303992
NM_001382658.3:c.1106C>T