Canonical Allele Identifier: PA2826419586
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.His18916Arg
CA349470323
NM_001256850.1:c.56747A>G