Canonical Allele Identifier: PA658667010
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467490
ClinVar RCV Id: RCV000734884 RCV001079343 RCV001135500 RCV001135501 RCV001135502 RCV001135503 RCV001135499 RCV002341353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg25537His
CA1989884
NM_001267550.2:c.76610G>A