Canonical Allele Identifier: PA2830217847
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Trp12864Arg
CA1991706
NM_133432.3:c.38590T>C
CA349434242
NM_133432.3:c.38590T>A