Allele Registry

Canonical Allele Identifier: PA3057313099

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV004697595

ClinVar Variation:

3337093

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Arg546Gln	CA10568427 NM_000132.4:c.1637G>A