Canonical Allele Identifier: PA2830228708
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1780433
ClinVar RCV Id: RCV002410026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Met601Thr
CA349505971
NM_133437.4:c.1802T>C