Canonical Allele Identifier: PA105217
Gene: F8 HGNC NCBI
ClinVar Allele:
25262
ClinVar RCV:
RCV000010936
ClinVar Variation:
10223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg550Cys
CA255113
NM_000132.4:c.1648C>T