Canonical Allele Identifier: PA915958329
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 811122
ClinVar RCV Id: RCV001000774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000123.1:p.Leu480Pro
CA414914273
NM_000132.4:c.1439T>C