Allele Registry

Canonical Allele Identifier: PA2825051086

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV003393027

ClinVar Variation:

2635321

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ser2192Arg	CA414906517 NM_000132.4:c.6576T>G CA414906518 NM_000132.4:c.6576T>A CA414906786 NM_000132.4:c.6574A>C