Allele Registry

Canonical Allele Identifier: PA916071823

Gene: F8 HGNC NCBI

ClinVar Allele:

25356

ClinVar RCV:

RCV000011030

ClinVar Variation:

10317

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Thr38Ile	CA255210 NM_019863.3:c.113C>T