Canonical Allele Identifier: PA2830195580
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg13660His
CA309929
NM_133378.4:c.40979G>A