Canonical Allele Identifier: PA2830211427
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Leu2127Val
CA2005016
NM_133432.3:c.6379T>G