Canonical Allele Identifier: PA2826500793
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12076
ClinVar RCV Id: RCV000012857 RCV000851974 RCV002243638 RCV002496330 RCV001091742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254483.1:p.Ala270Val
CA121850
NM_001267554.1:c.809C>T