Canonical Allele Identifier: PA106595
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10156
ClinVar RCV Id: RCV000010869 RCV002247317
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Gly41Cys
CA255048
NM_000132.4:c.121G>T