Canonical Allele Identifier: PA238311
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu1004Lys
CA238309
NM_001267550.2:c.3010G>A