Canonical Allele Identifier: PA645411751
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332742
ClinVar RCV Id: RCV000303011 RCV000343285 RCV000357853 RCV000394606 RCV000404006 RCV000471925 RCV001531503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala28995Thr
CA1988398
NM_001267550.2:c.86983G>A