Canonical Allele Identifier: PA2826496519
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_001254479.2:p.Val14759Phe
CA349645132
NM_001267550.2:c.44275G>T