Canonical Allele Identifier: PA2826428497
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg33218Trp
CA60956099
NM_001256850.1:c.99652C>T