Canonical Allele Identifier: PA2829444288
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47639
ClinVar RCV Id: RCV000040908 RCV000246329 RCV000769857 RCV000713950 RCV001131492 RCV001131493 RCV001134484 RCV000852780 RCV001131495 RCV001079468 RCV001131494 RCV002227931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val24824Ile
CA231620
NM_003319.4:c.74470G>A