Allele Registry

Canonical Allele Identifier: PA103395

Gene: F5 HGNC NCBI

ClinVar RCV:

RCV000000683

RCV003595850

ClinVar Variation:

649

HGVS (amino-acid)	Matching Registered Transcripts
NP_000121.2:p.Tyr1730Cys	CA251551 NM_000130.5:c.5189A>G