Canonical Allele Identifier: PA109124
Gene: F8 HGNC NCBI
ClinVar Allele:
25228
ClinVar RCV:
RCV000010902
ClinVar Variation:
10189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Val285Gly
CA255076
NM_000132.4:c.854T>G