Allele Registry

Canonical Allele Identifier: PA2573061410

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV001803547

ClinVar Variation:

1330455

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg1740Met	CA414913424 NM_000132.4:c.5219G>T