Allele Registry

Canonical Allele Identifier: PA3057313032

Gene: F8 HGNC NCBI

ClinVar RCV:

RCV004746624

ClinVar Variation:

3356191

HGVS (amino-acid)	Matching Registered Transcripts
NP_000123.1:p.Gly41Ser	CA10568644 NM_000132.4:c.121G>A