Canonical Allele Identifier: PA2741849692
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2921699
ClinVar RCV Id: RCV003782721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly35340Val
CA349407206
NM_001267550.2:c.106019G>T