Canonical Allele Identifier: PA2830190668
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202783
ClinVar RCV Id: RCV000289199 RCV000340841 RCV000304650 RCV000344680 RCV000344293 RCV000407072 RCV000557548 RCV001170665 RCV000726007 RCV002415796 RCV004539721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp796Asn
CA310273
NM_133378.4:c.2386G>A