Canonical Allele Identifier: PA104688
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10246
ClinVar RCV Id: RCV000010959 RCV000852072 RCV001560529 RCV002490351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ala723Thr
CA255138
NM_000132.4:c.2167G>A