Canonical Allele Identifier: PA106306
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10270
ClinVar RCV Id: RCV000010983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Gly1769Arg
CA255158
NM_000132.4:c.5305G>A
CA414910833
NM_000132.4:c.5305G>C