Canonical Allele Identifier: PA2826428117
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu32885Gln
CA309135
NM_001256850.1:c.98653G>C