Canonical Allele Identifier: PA913191599
Gene: CYP2D6 HGNC NCBI
ClinVar RCV:
RCV000734618
ClinVar Variation:
39385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000097.3:p.His324Pro
CA10264758
NM_000106.6:c.971A>C