Canonical Allele Identifier: PA140408
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47234
ClinVar RCV Id: RCV000040504 RCV000184735 RCV000765558 RCV001088816 RCV002321531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr20490Ala
CA140405
NM_001256850.1:c.61468A>G