Canonical Allele Identifier: PA2826410721
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg1421Trp
CA181985
NM_001256850.1:c.4261C>T