Canonical Allele Identifier: PA311108
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203056
ClinVar RCV Id: RCV000283303 RCV000340707 RCV000392156 RCV000537271 RCV000617715 RCV000305798 RCV000353303 RCV000764297 RCV000713947 RCV001270047 RCV002282014 RCV003486756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu33483Gln
CA311106
NM_001267550.2:c.100447G>C