Canonical Allele Identifier: PA2829907310
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10126
ClinVar RCV Id: RCV000010839 RCV000851861 RCV001169905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Arg191Gln
CA255027
NM_019863.3:c.572G>A