Allele Registry

Canonical Allele Identifier: PA645430164

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV000333070

RCV000884570

ClinVar Variation:

304821

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Arg543Leu	CA5967330 NM_000506.5:c.1628G>T