Canonical Allele Identifier: PA105287
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10245
ClinVar RCV Id: RCV000010958 RCV000851590 RCV000851937 RCV002247321 RCV002281701 RCV002490350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg717Trp
CA255137
NM_000132.4:c.2149C>T