Allele Registry

Canonical Allele Identifier: PA645430135

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV000243525

RCV000306522

RCV000396446

RCV001610577

ClinVar Variation:

256317

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Thr165Met	CA5966962 NM_000506.5:c.494C>T