Canonical Allele Identifier: PA105229
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10224
ClinVar RCV Id: RCV000010937 RCV000757245
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg550Gly
CA255114
NM_000132.4:c.1648C>G