Canonical Allele Identifier: PA2829904369
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2364529
ClinVar RCV Id: RCV002984443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_062562.1:p.Val273Ile
CA256461508
NM_019616.4:c.817G>A