Allele Registry

Canonical Allele Identifier: PA1139733736

Gene: F8 HGNC NCBI

ClinVar Allele:

982306

ClinVar RCV:

RCV001285320

RCV003399053

RCV003987825

ClinVar Variation:

993637

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Tyr40del	CA1139667895 NM_019863.3:c.118_120del