Canonical Allele Identifier: PA645412270
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg32077Gln
CA1986795
NM_001267550.2:c.96230G>A