Canonical Allele Identifier: PA141669
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu34789Lys
CA141665
NM_001267550.2:c.104365G>A