Allele Registry

Canonical Allele Identifier: PA105322

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000011007

ClinVar Variation:

10294

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Asn1941Ser	CA255184 NM_000132.4:c.5822A>G