Canonical Allele Identifier: PA2829433779
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val7860Ala
CA309980
NM_003319.4:c.23579T>C