Canonical Allele Identifier: PA2826422797
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Met24721Thr
CA1989527
NM_001256850.1:c.74162T>C