Canonical Allele Identifier: PA309018
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu11534Pro
CA309016
NM_001267550.2:c.34601T>C