Canonical Allele Identifier: PA2573068650
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1329220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val31571Met
CA60972536
NM_001267550.2:c.94711G>A