Allele Registry

Canonical Allele Identifier: PA645294496

Gene: F5 HGNC NCBI

ClinVar RCV:

RCV000282679

RCV000293300

RCV000350323

RCV000374642

RCV004021372

ClinVar Variation:

293602

HGVS (amino-acid)	Matching Registered Transcripts
NP_000121.2:p.Gly1317Ser	CA1233789 NM_000130.5:c.3949G>A