Canonical Allele Identifier: PA2826416628
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.His13271Tyr
CA1995587
NM_001256850.1:c.39811C>T