Canonical Allele Identifier: PA108490
Gene: F8 HGNC NCBI
ClinVar Allele:
25356
ClinVar RCV:
RCV000011030
ClinVar Variation:
10317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Thr2173Ile
CA255210
NM_000132.4:c.6518C>T