Canonical Allele Identifier: PA2826418798
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile17440Thr
CA237918
NM_001256850.1:c.52319T>C