Allele Registry

Canonical Allele Identifier: PA097424

Gene: F2 HGNC NCBI

ClinVar RCV:

RCV002468928

ClinVar Variation:

13307

HGVS (amino-acid)	Matching Registered Transcripts
NP_000497.1:p.Met380Thr	CA123011 NM_000506.5:c.1139T>C