Canonical Allele Identifier: PA2580105392
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2318048
ClinVar RCV Id: RCV002888616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Ser2273Asn
CA10567755
NM_000132.4:c.6818G>A