Canonical Allele Identifier: PA106294
Gene: F8 HGNC NCBI
ClinVar Allele:
25214
ClinVar RCV:
RCV000010888
ClinVar Variation:
10175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Gly164Val
CA255064
NM_000132.4:c.491G>T