Allele Registry

Canonical Allele Identifier: PA2499228724

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV001420467

ClinVar Variation:

1098533

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Trp1048Cys	CA414898457 NM_000132.4:c.3144G>T CA414898458 NM_000132.4:c.3144G>C