Canonical Allele Identifier: PA302382
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191811
ClinVar RCV Id: RCV000172150 RCV000412707 RCV000459823 RCV001129589 RCV001129591 RCV001129590 RCV001129592 RCV001129593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg35164Cys
CA302379
NM_001267550.2:c.105490C>T