Canonical Allele Identifier: PA106244
Gene: F8 HGNC NCBI
ClinVar Allele:
25286
ClinVar RCV:
RCV000010960
ClinVar Variation:
10247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Glu739Lys
CA255139
NM_000132.4:c.2215G>A