Canonical Allele Identifier: PA107430
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10167
ClinVar RCV Id: RCV000010880 RCV000508582 RCV002247318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Lys108Thr
CA255056
NM_000132.4:c.323A>C