Allele Registry

Canonical Allele Identifier: PA107043

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010921

ClinVar Variation:

10208

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ile405Ser	CA255098 NM_000132.4:c.1214T>G