Canonical Allele Identifier: PA2826422137
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.His23424Arg
CA1990089
NM_001256850.1:c.70271A>G