Canonical Allele Identifier: PA2825049538
Gene: F5 HGNC NCBI

Linked Data

ClinVar Variation Id: 3091480
ClinVar RCV Id: RCV004385866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Asn328His
CA343132285
NM_000130.5:c.982A>C