Allele Registry

Canonical Allele Identifier: PA103443

Gene: F7 HGNC NCBI

ClinVar RCV:

RCV000852243

RCV000995102

RCV002245661

RCV002487578

ClinVar Variation:

627403

HGVS (amino-acid)	Matching Registered Transcripts
NP_000122.1:p.Ala304Val	CA7060164 NM_000131.4:c.911C>T