Canonical Allele Identifier: PA106565
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10187
ClinVar RCV Id: RCV000010900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Gly278Arg
CA255074
NM_000132.4:c.832G>A
CA414918292
NM_000132.4:c.832G>C