Canonical Allele Identifier: PA255105
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10214
ClinVar RCV Id: RCV000010927
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Tyr473His
CA255104
NM_000132.4:c.1417T>C