Allele Registry

Canonical Allele Identifier: PA913194268

Gene: F8 HGNC NCBI

ClinVar Allele:

25354

ClinVar RCV:

RCV000011028

RCV000851846

RCV003147281

ClinVar Variation:

10315

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Arg34His	CA255208 NM_019863.3:c.101G>A