Canonical Allele Identifier: PA2826411363
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47431
ClinVar RCV Id: RCV000040700 RCV000172460 RCV000242133 RCV000287099 RCV000347654 RCV000403204 RCV000309186 RCV000339655 RCV000463035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg2540His
CA140973
NM_001256850.1:c.7619G>A