Canonical Allele Identifier: PA141280
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47531
ClinVar RCV Id: RCV000040800 RCV000172195 RCV001087420 RCV002371845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val28555Leu
CA141278
NM_133378.4:c.85663G>C