Canonical Allele Identifier: PA139827
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47036
ClinVar RCV Id: RCV000040306 RCV000082412 RCV000282058 RCV000278424 RCV000318292 RCV000321923 RCV000376541 RCV000618761 RCV000770020 RCV000852849 RCV001084198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser16640Thr
CA139823
NM_001267550.2:c.49919G>C