Canonical Allele Identifier: PA2580124632
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2295729
ClinVar RCV Id: RCV002849901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000495.1:p.Ala457Thr
CA7060736
NM_000504.4:c.1369G>A