Allele Registry

Canonical Allele Identifier: PA108113

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV002249964

RCV002471264

ClinVar Variation:

1685797

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Pro947Arg	CA10568278 NM_000132.4:c.2840C>G