Canonical Allele Identifier: PA311137
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203066
ClinVar RCV Id: RCV000185086 RCV000530236 RCV001704936 RCV002390481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg32534Gln
CA311136
NM_001256850.1:c.97601G>A