Canonical Allele Identifier: PA105192
Gene: F8 HGNC NCBI
ClinVar Allele:
792180
ClinVar RCV:
RCV000991026
ClinVar Variation:
804141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg490Gly
CA414912841
NM_000132.4:c.1468A>G