Canonical Allele Identifier: PA283807
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47365
ClinVar RCV Id: RCV000040635 RCV000252219 RCV000472312 RCV001092342 RCV000770124 RCV001131190 RCV001131191 RCV001131192 RCV001131193 RCV001131194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg2354His
CA283801
NM_133379.5:c.7061G>A