Canonical Allele Identifier: PA645411415
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 284294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro27661Ser
CA1988990
NM_001267550.2:c.82981C>T