Canonical Allele Identifier: PA2826946905
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10585
ClinVar RCV Id: RCV000011331 RCV000851602 RCV001390296 RCV002284168 RCV002247326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001300842.1:p.Arg153His
CA255342
NM_001313913.2:c.458G>A