Canonical Allele Identifier: PA105791
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10351
ClinVar RCV Id: RCV000011064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Cys198Gly
CA255227
NM_000132.4:c.592T>G