Canonical Allele Identifier: PA183599
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179043
ClinVar RCV Id: RCV000155827 RCV000476685 RCV000733639 RCV000769975 RCV002345509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg19036Gln
CA183598
NM_133378.4:c.57107G>A