Canonical Allele Identifier: PA2826491538
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238716
ClinVar RCV Id: RCV000229056 RCV001509201 RCV002408963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr678Ala
CA10581905
NM_001267550.2:c.2032A>G