Canonical Allele Identifier: PA1139668297
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 988832
ClinVar RCV Id: RCV001270526 RCV001420418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Gly442Asp
CA388794263
NM_000504.4:c.1325G>A