Canonical Allele Identifier: PA2826418539
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501103
ClinVar RCV Id: RCV000597499 RCV000643805 RCV003150293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr16954Arg
CA1993387
NM_001256850.1:c.50861C>G