Canonical Allele Identifier: PA104913
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10321
ClinVar RCV Id: RCV000011034 RCV002247323
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Arg2182Cys
CA255214
NM_000132.4:c.6544C>T