Canonical Allele Identifier: PA108833
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10310
ClinVar RCV Id: RCV000011023 RCV001508071
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Tyr2124Cys
CA255203
NM_000132.4:c.6371A>G