Allele Registry

Canonical Allele Identifier: PA645294755

Gene: F12 HGNC NCBI

ClinVar RCV:

RCV000322122

RCV000355853

RCV000860986

RCV004555554

ClinVar Variation:

353001

HGVS (amino-acid)	Matching Registered Transcripts
NP_000496.2:p.Leu140Val	CA3581488 NM_000505.4:c.418C>G