Canonical Allele Identifier: PA2826422279
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg23703Trp
CA1989963
NM_001256850.1:c.71107C>T