Allele Registry

Canonical Allele Identifier: PA108258

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000851606

RCV001267618

RCV001803794

RCV002248743

RCV002476015

RCV003103799

ClinVar Variation:

439683

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Ser2030Asn	CA10567911 NM_000132.4:c.6089G>A