Canonical Allele Identifier: PA237592
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile35744Val
CA237590
NM_001267550.2:c.107230A>G