Canonical Allele Identifier: PA309567
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile9604Thr
CA309566
NM_001256850.1:c.28811T>C