Canonical Allele Identifier: PA103361
Gene: F5 HGNC NCBI
ClinVar RCV:
RCV000000678
ClinVar Variation:
644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Arg334Thr
CA251546
NM_000130.5:c.1001G>C