Canonical Allele Identifier: PA2830220117
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467495
ClinVar RCV Id: RCV000533551 RCV001563336 RCV002341354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr16661Met
CA1989858
NM_133432.3:c.49982C>T