Canonical Allele Identifier: PA104791
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10110
ClinVar RCV Id: RCV000010822 RCV000756109
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg1960Gln
CA255019
NM_000132.4:c.5879G>A