Canonical Allele Identifier: PA104724
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10268
ClinVar RCV Id: RCV000010981 RCV003114183
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg1715Gly
CA255157
NM_000132.4:c.5143C>G