Canonical Allele Identifier: PA311953
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met7111Thr
CA311951
NM_001267550.2:c.21332T>C