Canonical Allele Identifier: PA915958456
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 627088
ClinVar RCV Id: RCV000851815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Val1722Met
CA414913665
NM_000132.4:c.5164G>A