Canonical Allele Identifier: PA107961
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10316
ClinVar RCV Id: RCV000011029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Pro2172Gln
CA255209
NM_000132.4:c.6515C>A