Canonical Allele Identifier: PA104772
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10274
ClinVar RCV Id: RCV000010987 RCV001552643 RCV003430635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg1800His
CA255162
NM_000132.4:c.5399G>A