Canonical Allele Identifier: PA2829904427
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 883022
ClinVar RCV Id: RCV001113154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_062562.1:p.Leu439Pro
CA388787213
NM_019616.4:c.1316T>C