Canonical Allele Identifier: PA1139687028
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 862399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu35349Ile
CA349407153
NM_001267550.2:c.106045C>A