Canonical Allele Identifier: PA916065129
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46972
ClinVar RCV Id: RCV000040242 RCV000463518 RCV000725048 RCV000852859 RCV001130918 RCV001130920 RCV001130919 RCV001130921 RCV001130917 RCV001171013 RCV002399389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser5691Thr
CA139670
NM_133437.4:c.17071T>A