Canonical Allele Identifier: PA106688
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10217
ClinVar RCV Id: RCV000010930 RCV000851700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Gly498Arg
CA255109
NM_000132.4:c.1492G>A
CA414912741
NM_000132.4:c.1492G>C