Canonical Allele Identifier: PA105096
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10192
ClinVar RCV Id: RCV000010905 RCV000255290
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg301His
CA255079
NM_000132.4:c.902G>A