Allele Registry

Canonical Allele Identifier: PA1139670100

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV001285264

ClinVar Variation:

993612

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Val99Ala	CA414920067 NM_000132.4:c.296T>C