Canonical Allele Identifier: PA2826490936
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val70Met
CA2006391
NM_001267550.2:c.208G>A