Canonical Allele Identifier: PA311024
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly32481Glu
CA311022
NM_001267550.2:c.97442G>A