Canonical Allele Identifier: PA211177
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46603
ClinVar RCV Id: RCV000039873 RCV000126097 RCV001082361 RCV001134549 RCV001134550 RCV001134551 RCV001134552 RCV001170871 RCV001131551 RCV002225075 RCV004534852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gln5188Pro
CA211174
NM_001267550.2:c.15563A>C