Allele Registry

Canonical Allele Identifier: PA916071877

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011037

ClinVar Variation:

10324

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Arg93Leu	CA340964 NM_019863.3:c.278G>T