Canonical Allele Identifier: PA2826417168
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile14407Thr
CA1994912
NM_001256850.1:c.43220T>C