Canonical Allele Identifier: PA2826500790
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 311228
ClinVar RCV Id: RCV000345888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254483.1:p.Ala268Thr
CA7060207
NM_001267554.1:c.802G>A