Canonical Allele Identifier: PA2829439248
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Met17297Thr
CA1989527
NM_003319.4:c.51890T>C