Canonical Allele Identifier: PA309096
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly24838Ala
CA309094
NM_001267550.2:c.74513G>C