Canonical Allele Identifier: PA107330
Gene: F8 HGNC NCBI
ClinVar Allele:
25238
ClinVar RCV:
RCV000010912
ClinVar Variation:
10199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Leu327Pro
CA255086
NM_000132.4:c.980T>C