Allele Registry

Canonical Allele Identifier: PA916071862

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV000010840

ClinVar Variation:

10127

HGVS (amino-acid)	Matching Registered Transcripts
NP_063916.1:p.Leu50Ser	CA255028 NM_019863.3:c.149T>C