Canonical Allele Identifier: PA2826422802
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val24728Ile
CA1989522
NM_001256850.1:c.74182G>A