Canonical Allele Identifier: PA2830217093
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.His11617Arg
CA349470323
NM_133432.3:c.34850A>G