Canonical Allele Identifier: PA913194268
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10315
ClinVar RCV Id: RCV000011028 RCV000851846 RCV003147281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Arg34His
CA255208
NM_019863.3:c.101G>A