Canonical Allele Identifier: PA139577
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46938
ClinVar RCV Id: RCV000040208 RCV000171326 RCV000643604 RCV001134753 RCV001134755 RCV001134754 RCV001134751 RCV001134752 RCV001293182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val1099Met
CA139572
NM_133379.5:c.3295G>A