Canonical Allele Identifier: PA915958638
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 627123
ClinVar RCV Id: RCV000851860 RCV001803975
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Pro2311His
CA337319439
NM_000132.4:c.6932C>A