Canonical Allele Identifier: PA916066988
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_597681.4:p.Thr9722Arg
CA1993387
NM_133437.4:c.29165C>G