Canonical Allele Identifier: PA2830220500
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu17362Asp
CA1989554
NM_133432.3:c.52086A>C
CA349600653
NM_133432.3:c.52086A>T