Allele Registry

Canonical Allele Identifier: PA108334

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010919

ClinVar Variation:

10206

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ser392Pro	CA255096 NM_000132.4:c.1174T>C