Canonical Allele Identifier: PA284308
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47684
ClinVar RCV Id: RCV000040953 RCV000245839 RCV000299511 RCV000357713 RCV000302886 RCV000398040 RCV000398033 RCV000461324 RCV000993378
ClinVar Variation Id: 518882
ClinVar RCV Id: RCV000621956 RCV001860374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu32492Asp
CA284306
NM_133378.4:c.97476G>C
CA349409323
NM_133378.4:c.97476G>T