Canonical Allele Identifier: PA2830190600
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1780433
ClinVar RCV Id: RCV002410026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Met647Thr
CA349505971
NM_133378.4:c.1940T>C