Allele Registry

Canonical Allele Identifier: PA108374

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010942

ClinVar Variation:

10229

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ser577Phe	CA255120 NM_000132.4:c.1730C>T