Canonical Allele Identifier: PA282701
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46614
ClinVar RCV Id: RCV000039884 RCV000242487 RCV000293024 RCV000333991 RCV000318931 RCV000387402 RCV000387868 RCV000458298 RCV000770101 RCV000852911 RCV001529446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val5118Met
CA282698
NM_001256850.1:c.15352G>A