Canonical Allele Identifier: PA658667228
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro26821Leu
CA1989341
NM_001267550.2:c.80462C>T