Canonical Allele Identifier: PA2826489384
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405144

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg1431Trp
CA2005344
NM_001267550.2:c.4291C>T