Canonical Allele Identifier: PA140182
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47163
ClinVar RCV Id: RCV000040433 RCV000172653 RCV000286181 RCV000280109 RCV000337757 RCV000343483 RCV000396846 RCV001086697 RCV002222151 RCV001171297 RCV002321530 RCV004534913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu18600Gln
CA140179
NM_001256850.1:c.55798G>C