Canonical Allele Identifier: PA916071821
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10316
ClinVar RCV Id: RCV000011029
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Pro37Gln
CA255209
NM_019863.3:c.110C>A