Allele Registry

Canonical Allele Identifier: PA2580105356

Gene: F8 HGNC NCBI

ClinVar Allele:

1704292

ClinVar RCV:

RCV002284346

ClinVar Variation:

1705972

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ala1939Glu	CA414906727 NM_000132.4:c.5816C>A