Canonical Allele Identifier: PA185555
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179976
ClinVar RCV Id: RCV000156779 RCV000863658 RCV001447793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys612Glu
CA185553
NM_001267550.2:c.1834A>G