Allele Registry

Canonical Allele Identifier: PA645294596

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000442362

ClinVar Variation:

381561

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Val2035Met	CA16609159 NM_000132.4:c.6103G>A