Canonical Allele Identifier: PA149422
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96278
ClinVar RCV Id: RCV000082388 RCV000462914 RCV000852943 RCV000617419 RCV001133516 RCV001133518 RCV001133520 RCV001133517 RCV001133519 RCV001811386 RCV003486639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg922His
CA149418
NM_001267550.2:c.2765G>A