Canonical Allele Identifier: PA247914
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 198970
ClinVar RCV Id: RCV000222950 RCV000286098 RCV000280133 RCV000329768 RCV000335156 RCV000392294 RCV000724263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys8648Glu
CA247912
NM_001267550.2:c.25942A>G