Allele Registry

Canonical Allele Identifier: PA123024

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV002468931

ClinVar Variation:

13313

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Arg425His	CA123022 NM_000506.5:c.1274G>A