Canonical Allele Identifier: PA139881
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47057
ClinVar RCV Id: RCV000040327 RCV000227290 RCV000250975 RCV000279940 RCV000294783 RCV000334677 RCV000389173 RCV000374388 RCV000725456 RCV001170610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser14702Ile
CA139879
NM_133378.4:c.44105G>T