Canonical Allele Identifier: PA342810
Gene: F2 HGNC NCBI
ClinVar Allele:
40578
ClinVar RCV:
RCV000024607
ClinVar Variation:
31922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000497.1:p.Arg596Leu
CA342808
NM_000506.5:c.1787G>T