Allele Registry

Canonical Allele Identifier: PA2573061401

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV001802583

ClinVar Variation:

1330924

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ile494Ser	CA414912795 NM_000132.4:c.1481T>G