Allele Registry

Canonical Allele Identifier: PA097293

Gene: F12 HGNC NCBI

ClinVar RCV:

RCV000001229

RCV000414902

RCV001198361

ClinVar Variation:

1170

HGVS (amino-acid)	Matching Registered Transcripts
NP_000496.2:p.Thr328Arg	CA114819 NM_000505.4:c.983C>G