Canonical Allele Identifier: PA108776
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10115
ClinVar RCV Id: RCV000010828 RCV002508187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Tyr1699Phe
CA255022
NM_000132.4:c.5096A>T