Allele Registry

Canonical Allele Identifier: PA2499232972

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV001420451

ClinVar Variation:

1098517

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Ser203Gly	CA380264757 NM_000506.5:c.607A>G