Canonical Allele Identifier: PA105126
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10111
ClinVar RCV Id: RCV000010823 RCV000757254 RCV000852002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg391His
CA120918
NM_000132.4:c.1172G>A