Canonical Allele Identifier: PA2826500825
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 12088
ClinVar RCV Id: RCV000012869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254483.1:p.His324Gln
CA121870
NM_001267554.1:c.972T>G
CA388786802
NM_001267554.1:c.972T>A