Canonical Allele Identifier: PA181921
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178252
ClinVar RCV Id: RCV000154992 RCV000247714 RCV000228841 RCV000713979 RCV001353378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Cys4696Arg
CA181920
NM_133378.4:c.14086T>C