Canonical Allele Identifier: PA141352
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47561
ClinVar RCV Id: RCV000040830 RCV000172615 RCV000270075 RCV000292373 RCV000349608 RCV000327509 RCV000380825 RCV000621105 RCV000769875 RCV000852785 RCV001085084 RCV004534945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala31885Thr
CA141349
NM_001267550.2:c.95653G>A