Canonical Allele Identifier: PA174862
Gene: VKORC1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161827
ClinVar RCV Id: RCV000149363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271271.1:p.Arg128Leu
CA174861
NM_001284342.3:c.383G>T