Allele Registry

Canonical Allele Identifier: PA107547

Gene: F8 HGNC NCBI

ClinVar Variation Id: 10280

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Met1842Ile	CA255169 NM_000132.4:c.5526G>A CA414908618 NM_000132.4:c.5526G>T CA414908619 NM_000132.4:c.5526G>C