Canonical Allele Identifier: PA121842
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 12059
ClinVar RCV Id: RCV000012839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Arg287Trp
CA121840
NM_000504.4:c.859A>T