Canonical Allele Identifier: PA309084
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly22910Arg
CA309082
NM_001267550.2:c.68728G>A
CA349671294
NM_001267550.2:c.68728G>C