Canonical Allele Identifier: PA2826428734
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr33446Met
CA344687
NM_001256850.1:c.100337C>T