Canonical Allele Identifier: PA107902
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10281
ClinVar RCV Id: RCV000010994 RCV000851817
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Pro1844Ser
CA255170
NM_000132.4:c.5530C>T