Canonical Allele Identifier: PA2826413928
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332911
ClinVar RCV Id: RCV000286579 RCV000290510 RCV000347856 RCV000378580 RCV000378033 RCV000997528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly7736Ser
CA2000493
NM_001256850.1:c.23206G>A