Canonical Allele Identifier: PA2826425597
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 504537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Met29395Thr
CA1987355
NM_001256850.1:c.88184T>C