Canonical Allele Identifier: PA658654648
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 444838
ClinVar RCV Id: RCV000513611 RCV001169190 RCV002476025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Leu1481Pro
CA10568107
NM_000132.4:c.4442T>C