Allele Registry

Canonical Allele Identifier: PA097301

Gene: F12 HGNC NCBI

ClinVar RCV:

RCV000001228

RCV000222890

RCV000255869

RCV000763138

ClinVar Variation:

1169

HGVS (amino-acid)	Matching Registered Transcripts
NP_000496.2:p.Thr328Lys	CA114817 NM_000505.4:c.983C>A