Canonical Allele Identifier: PA107062
Gene: F8 HGNC NCBI
ClinVar Allele:
25255
ClinVar RCV:
RCV000010929
ClinVar Variation:
10216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ile494Thr
CA255108
NM_000132.4:c.1481T>C