Canonical Allele Identifier: PA247913
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_596869.4:p.Lys7404Glu
CA247912
NM_133378.4:c.22210A>G