Canonical Allele Identifier: PA645411588
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg28326Trp
CA1988713
NM_001267550.2:c.84976C>T