Canonical Allele Identifier: PA140663
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47315
ClinVar RCV Id: RCV000040585 RCV000539387 RCV000727443 RCV002362634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Thr2160Ala
CA140658
NM_133379.5:c.6478A>G