Canonical Allele Identifier: PA181607
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96321
ClinVar RCV Id: RCV000154885 RCV000229045 RCV000620292 RCV001130049 RCV000852784 RCV001130045 RCV001130046 RCV001130047 RCV001130048 RCV001811391 RCV003486647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile32497Thr
CA181603
NM_001267550.2:c.97490T>C