Canonical Allele Identifier: PA645294486
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 293609
ClinVar RCV Id: RCV000300358 RCV000299114 RCV000361040 RCV000402033 RCV002450839 RCV003949974 RCV003595921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Asp1134Glu
CA1233917
NM_000130.5:c.3402C>A
CA343118086
NM_000130.5:c.3402C>G