Canonical Allele Identifier: PA645387144
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 311281
ClinVar RCV Id: RCV000373557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Thr409Ile
CA7060708
NM_000504.4:c.1226C>T