Canonical Allele Identifier: PA658666017
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met19128Val
CA1993056
NM_001267550.2:c.57382A>G