Allele Registry

Canonical Allele Identifier: PA3057546639

Gene: F8 HGNC NCBI

ClinVar Allele:

3883038

ClinVar RCV:

RCV005234571

ClinVar Variation:

3766876

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ile1940Thr	CA414906699 NM_000132.4:c.5819T>C