Canonical Allele Identifier: PA139507
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46913
ClinVar RCV Id: RCV000040183 RCV000456345 RCV000714011 RCV002433513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val1045Met
CA139502
NM_133379.5:c.3133G>A