Canonical Allele Identifier: PA645410139
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229458
ClinVar RCV Id: RCV000222321 RCV000550187 RCV000997454 RCV001136502 RCV001136503 RCV001136504 RCV001136505 RCV001136506 RCV002429076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg17618His
CA1993917
NM_001267550.2:c.52853G>A