Canonical Allele Identifier: PA112606
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 12655
ClinVar RCV Id: RCV000013491 RCV002513012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala743Val
CA256505
NM_001256850.1:c.2228C>T