Canonical Allele Identifier: PA2829437631
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202827
ClinVar RCV Id: RCV000643517 RCV000764321 RCV001721160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr14459Ala
CA310409
NM_003319.4:c.43375A>G