Canonical Allele Identifier: PA2830226767
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr26053Met
CA311202
NM_133432.3:c.78158C>T