Allele Registry

Canonical Allele Identifier: PA104734

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV003991908

ClinVar Variation:

3068228

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg1740Gly	CA414913430 NM_000132.4:c.5218A>G