Allele Registry

Canonical Allele Identifier: PA2825051079

Gene: F8 HGNC NCBI

ClinVar Allele:

982306

ClinVar RCV:

RCV001285320

RCV003399053

RCV003987825

ClinVar Variation:

993637

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Tyr2175del	CA1139667895 NM_000132.4:c.6523_6525del