Canonical Allele Identifier: PA141677
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47672
ClinVar RCV Id: RCV000040941 RCV002399393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34805Leu
CA141674
NM_001267550.2:c.104414G>T