Canonical Allele Identifier: PA178752
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165982
ClinVar RCV Id: RCV000152315 RCV002433666 RCV002483317 RCV001798482 RCV000539449 RCV000727083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg17968His
CA178750
NM_001267550.2:c.53903G>A