Canonical Allele Identifier: PA311179
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203080
ClinVar RCV Id: RCV000467913 RCV000595276 RCV000726382 RCV002399690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg33164Gln
CA311178
NM_001256850.1:c.99491G>A