Canonical Allele Identifier: PA104761
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10276
ClinVar RCV Id: RCV000010989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg1800Gly
CA255164
NM_000132.4:c.5398C>G