Canonical Allele Identifier: PA658665320
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467028
ClinVar RCV Id: RCV000544688 RCV001130792 RCV001130794 RCV001130796 RCV001130793 RCV001130795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala11111Thr
CA1998386
NM_001267550.2:c.33331G>A