Canonical Allele Identifier: PA2826491195
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val307Met
CA2006172
NM_001267550.2:c.919G>A