Canonical Allele Identifier: PA645410486
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264601
ClinVar RCV Id: RCV000242541 RCV000643435 RCV001131515 RCV001131516 RCV001131517 RCV000596820 RCV001128850 RCV001131514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg20531His
CA1992343
NM_001267550.2:c.61592G>A