Canonical Allele Identifier: PA2830205851
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332789
ClinVar RCV Id: RCV000280236 RCV000302427 RCV000342223 RCV000372071 RCV000403345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Trp21377Arg
CA1990582
NM_133378.4:c.64129T>C
CA349650430
NM_133378.4:c.64129T>A