Canonical Allele Identifier: PA658659133
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met35138Thr
CA1985265
NM_001267550.2:c.105413T>C