Canonical Allele Identifier: PA2830201760
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202989
ClinVar RCV Id: RCV000319148 RCV000268053 RCV000360353 RCV000377684 RCV000280857 RCV000643867 RCV001704928 RCV002271448 RCV002362960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp28296Asn
CA310905
NM_133378.4:c.84886G>A