Canonical Allele Identifier: PA114380
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 642
ClinVar RCV Id: RCV000000675 RCV000000676 RCV000023935 RCV000205002 RCV000454249 RCV000616414 RCV001095681 RCV001806997 RCV002399305 RCV003227589 RCV003493407 RCV003764502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Arg534Gln
CA114378
NM_000130.5:c.1601G>A