Canonical Allele Identifier: PA142038
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47849
ClinVar RCV Id: RCV000041118 RCV000462754 RCV001088266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile3470Thr
CA142036
NM_133437.4:c.10409T>C