Allele Registry

Canonical Allele Identifier: PA645294763

Gene: F12 HGNC NCBI

ClinVar RCV:

RCV000490384

RCV001529827

RCV004017499

ClinVar Variation:

225352

HGVS (amino-acid)	Matching Registered Transcripts
NP_000496.2:p.Ala343Pro	CA3581278 NM_000505.4:c.1027G>C