Canonical Allele Identifier: PA2830221025
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly18161Val
CA310647
NM_133432.3:c.54482G>T