Allele Registry

Canonical Allele Identifier: PA097416

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV002468927

ClinVar Variation:

13306

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Gly601Val	CA123009 NM_000506.5:c.1802G>T