Canonical Allele Identifier: PA2829432626
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1778491
ClinVar RCV Id: RCV002398830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val5694Phe
CA349645132
NM_003319.4:c.17080G>T