Canonical Allele Identifier: PA139534
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu13101Lys
CA139530
NM_001267550.2:c.39301G>A