Allele Registry

Canonical Allele Identifier: PA645294483

Gene: F5 HGNC NCBI

ClinVar RCV:

RCV000272741

RCV000273413

RCV000333121

RCV000368409

RCV003595922

ClinVar Variation:

293614

HGVS (amino-acid)	Matching Registered Transcripts
NP_000121.2:p.His1071Tyr	CA1233952 NM_000130.5:c.3211C>T