Canonical Allele Identifier: PA645294604
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 225353
ClinVar RCV Id: RCV000490278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Val2242Met
CA10567761
NM_000132.4:c.6724G>A