Canonical Allele Identifier: PA309014
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu10911Lys
CA309012
NM_001267550.2:c.32731G>A