Canonical Allele Identifier: PA916071850
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10318
ClinVar RCV Id: RCV000011031 RCV003103985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Arg43Cys
CA255211
NM_019863.3:c.127C>T