Canonical Allele Identifier: PA2580105337
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1878789
ClinVar RCV Id: RCV002511290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ile1681Thr
CA414914199
NM_000132.4:c.5042T>C