Canonical Allele Identifier: PA2830222328
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 513448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met20260Ile
CA1988293
NM_133432.3:c.60780G>C
CA349535308
NM_133432.3:c.60780G>T
CA349535311
NM_133432.3:c.60780G>A