Canonical Allele Identifier: PA104717
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10266
ClinVar RCV Id: RCV000010979 RCV000851813 RCV001091839 RCV003914826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg1708His
CA255154
NM_000132.4:c.5123G>A