Canonical Allele Identifier: PA311026
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile30841Thr
CA311025
NM_001256850.1:c.92522T>C