Allele Registry

Canonical Allele Identifier: PA107260

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010840

ClinVar Variation:

10127

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Leu2185Ser	CA255028 NM_000132.4:c.6554T>C