Canonical Allele Identifier: PA103347
Gene: F5 HGNC NCBI
ClinVar RCV:
RCV000000688
ClinVar Variation:
654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Arg2102Cys
CA251559
NM_000130.5:c.6304C>T