Canonical Allele Identifier: PA126957
Gene: CYP2D6 HGNC NCBI

Linked Data

ClinVar Variation Id: 16893
ClinVar RCV Id: RCV000018389 RCV000603460 RCV000734607 RCV001029560 RCV001030444 RCV001093717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000097.3:p.Pro34Ser
CA126956
NM_000106.6:c.100C>T