Allele Registry

Canonical Allele Identifier: PA2573061392

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV001803537

ClinVar Variation:

1330445

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Glu30Gly	CA414920550 NM_000132.4:c.89A>G