Canonical Allele Identifier: PA2826429131
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser33863Thr
CA1985096
NM_001256850.1:c.101588G>C