Canonical Allele Identifier: PA106831
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10288
ClinVar RCV Id: RCV000011001 RCV003480027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.His1867Arg
CA255177
NM_000132.4:c.5600A>G