Allele Registry

Canonical Allele Identifier: PA2573061418

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV001802670

ClinVar Variation:

1331011

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Thr314Pro	CA414917836 NM_000132.4:c.940A>C