Canonical Allele Identifier: PA283679
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47276
ClinVar RCV Id: RCV000040546 RCV000228575 RCV000246133 RCV000288739 RCV000343753 RCV000378581 RCV000349248 RCV000404030 RCV000768946 RCV000852816 RCV002496648 RCV001528766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro20679Leu
CA283677
NM_133378.4:c.62036C>T