Canonical Allele Identifier: PA658813872
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val13268Phe
CA1996603
NM_001267550.2:c.39802G>T