Canonical Allele Identifier: PA645294482
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 293616
ClinVar RCV Id: RCV000285967 RCV000345503 RCV000380348 RCV000396759 RCV003595923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Asn969Ser
CA1234009
NM_000130.5:c.2906A>G