Canonical Allele Identifier: PA103383
Gene: F5 HGNC NCBI
ClinVar RCV:
RCV000000689
ClinVar Variation:
655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000121.2:p.Ile387Thr
CA251561
NM_000130.5:c.1160T>C