Canonical Allele Identifier: PA302947
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196653
ClinVar RCV Id: RCV000259176 RCV000724604 RCV000818971 RCV000852774 RCV002390431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val34271Ile
CA302944
NM_001267550.2:c.102811G>A