Canonical Allele Identifier: PA2829907316
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 993916
ClinVar RCV Id: RCV001286176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_063916.1:p.Glu206Lys
CA414896766
NM_019863.3:c.616G>A