Canonical Allele Identifier: PA2826420687
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165881
ClinVar RCV Id: RCV000152244 RCV000172276 RCV000768948 RCV001082358 RCV004532693 RCV002371999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg20841Trp
CA178574
NM_001256850.1:c.62521C>T