Allele Registry

Canonical Allele Identifier: PA916071857

Gene: F8 HGNC NCBI

ClinVar Allele:

25360

ClinVar RCV:

RCV000011034

RCV002247323

ClinVar Variation:

10321

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Arg47Cys	CA255214 NM_019863.3:c.139C>T