Canonical Allele Identifier: PA141190
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47497
ClinVar RCV Id: RCV000040766 RCV000082444 RCV000269727 RCV000320246 RCV000364179 RCV000310741 RCV000365525 RCV000617583 RCV000852796 RCV001083905 RCV001798194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg27611His
CA141188
NM_133378.4:c.82832G>A