Allele Registry

Canonical Allele Identifier: PA121858

Gene: F7 HGNC NCBI

ClinVar RCV:

RCV000012861

RCV000250547

RCV000391182

RCV000396014

ClinVar Variation:

12080

HGVS (amino-acid)	Matching Registered Transcripts
NP_062562.1:p.Arg391Gln	CA121855 NM_019616.4:c.1172G>A