Canonical Allele Identifier: PA645412809
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332687
ClinVar RCV Id: RCV000281757 RCV000321782 RCV000372813 RCV000578001 RCV000616776 RCV000577947 RCV003137937
ClinVar Variation Id: 1760755
ClinVar RCV Id: RCV002409974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala35128Val
CA1985269
NM_001267550.2:c.105383C>T
CA2580064928
NM_001267550.2:c.105383_105384delinsTG