Canonical Allele Identifier: PA106275
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10170
ClinVar RCV Id: RCV000010883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Gly130Arg
CA255059
NM_000132.4:c.388G>C
CA414919865
NM_000132.4:c.388G>A