Canonical Allele Identifier: PA104948
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10098
ClinVar RCV Id: RCV000010810 RCV000852189
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg2228Gln
CA255016
NM_000132.4:c.6683G>A