Canonical Allele Identifier: PA2829433179
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile6774Thr
CA309893
NM_003319.4:c.20321T>C