Canonical Allele Identifier: PA311903
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile6510Val
CA311901
NM_001267550.2:c.19528A>G