Canonical Allele Identifier: PA2826492057
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535490
ClinVar RCV Id: RCV000643497 RCV001132372 RCV001132368 RCV001132369 RCV001132370 RCV001132371 RCV002325259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys1129Arg
CA2005562
NM_001267550.2:c.3386A>G