Canonical Allele Identifier: PA916065114
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.His5649Arg
CA1995834
NM_133437.4:c.16946A>G