Canonical Allele Identifier: PA2826491779
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283320
ClinVar RCV Id: RCV000536704 RCV000392857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val871Leu
CA2005776
NM_001267550.2:c.2611G>T
CA349496292
NM_001267550.2:c.2611G>C