Canonical Allele Identifier: PA2830227362
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47712
ClinVar RCV Id: RCV000040981 RCV000231148 RCV000286567 RCV000253556 RCV000287599 RCV000347285 RCV000341504 RCV000395312 RCV000769842 RCV001529340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr26656Ile
CA284402
NM_133432.3:c.79967C>T