Canonical Allele Identifier: PA2830213696
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.His5582Arg
CA1995834
NM_133432.3:c.16745A>G