Allele Registry

Canonical Allele Identifier: PA2826500740

Gene: F7 HGNC NCBI

ClinVar RCV:

RCV000852243

RCV000995102

RCV002245661

RCV002487578

ClinVar Variation:

627403

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254483.1:p.Ala220Val	CA7060164 NM_001267554.1:c.659C>T