Canonical Allele Identifier: PA242129
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 195639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val16693Ile
CA242127
NM_001267550.2:c.50077G>A