Canonical Allele Identifier: PA310047
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202708
ClinVar RCV Id: RCV000184616 RCV000555766 RCV000764330 RCV001132953 RCV001132954 RCV001132012 RCV001132011 RCV001132013 RCV002453674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile16079Thr
CA310046
NM_001256850.1:c.48236T>C