Canonical Allele Identifier: PA658665770
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467225
ClinVar RCV Id: RCV000555019 RCV001130078 RCV001130079 RCV001130080 RCV001130081 RCV001130777 RCV001700146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg16866Lys
CA1994337
NM_001267550.2:c.50597G>A