Canonical Allele Identifier: PA183589
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179039
ClinVar RCV Id: RCV000155823 RCV000292921 RCV000352439 RCV000387336 RCV000643752 RCV000289428 RCV001798515 RCV000344162 RCV004546441 RCV002354376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu28356Met
CA183587
NM_001256850.1:c.85066T>A