Canonical Allele Identifier: PA178476
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165799
ClinVar RCV Id: RCV000152203 RCV000332173 RCV000260100 RCV000370450 RCV000274661 RCV000366979 RCV000643482 RCV000768909 RCV001704096 RCV002345480 RCV004544366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly24745Glu
CA178475
NM_133378.4:c.74234G>A